JPH05383B2 - - Google Patents

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Publication number
JPH05383B2
JPH05383B2 JP20843587A JP20843587A JPH05383B2 JP H05383 B2 JPH05383 B2 JP H05383B2 JP 20843587 A JP20843587 A JP 20843587A JP 20843587 A JP20843587 A JP 20843587A JP H05383 B2 JPH05383 B2 JP H05383B2
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JP
Japan
Prior art keywords
salt
weight
isomer
monometallic
amount
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
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JP20843587A
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Japanese (ja)
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JPS6450856A (en
Inventor
Eiji Ogata
Koji Ono
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Konishi Chemical Ind Co Ltd
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Konishi Chemical Ind Co Ltd
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Filing date
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Application filed by Konishi Chemical Ind Co Ltd filed Critical Konishi Chemical Ind Co Ltd
Priority to JP20843587A priority Critical patent/JPS6450856A/en
Priority to DE3890647A priority patent/DE3890647C2/en
Priority to PCT/JP1988/000813 priority patent/WO1989001469A1/en
Priority to GB8908173A priority patent/GB2216125B/en
Priority to DE19883890647 priority patent/DE3890647T1/en
Priority to US07/362,411 priority patent/US5097074A/en
Publication of JPS6450856A publication Critical patent/JPS6450856A/en
Publication of JPH05383B2 publication Critical patent/JPH05383B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

産業上の利用分野 本発明は、4,4′−ジヒドロキシジフエニルス
ルホン粗製品から高純度4,4′−ジヒドロキシジ
フエニルスルホンモノ金属塩を高収率で製造する
新規な方法に関する。 従来の技術 4,4′−ジヒドロキシジフエニルスルホン(以
下、4,4′体という)は、優れた耐熱性、耐酸化
性、耐光安定性等を有することから、近年ポリエ
ステル樹脂、エポキシ樹脂、ポリカーボネート樹
脂、ポリエーテルスルホン樹脂等の高分子化学工
業の分野において多用されるに至つている。この
場合、2,4′−ジヒドロキシジフエニルスルホン
(以下、2,4′体という)、トリヒドロキシトリフ
エニルジスルホン(以下、トリ体という)等の不
純物を含有する4,4′体を原料として合成した高
分子生成物は分子量が小さくなつて機械的性質が
低下する傾向があり、この傾向は2,4′体、トリ
体等の不純物が多い程顕著となる。従つて、2,
4′体、トリ体等の不純物ができる限り除去された
高純度の4,4′体の供給が要望されている。ま
た、4,4′体は、カラー写真用カツプラー原料、
感熱記録紙用顕色剤等としても有用であり、この
場合にも高純度であることが望ましい。 4,4′体は、工業的には主にフエノールと硫酸等
のスルホン化剤との脱水反応により製造されてお
り、反応生成物中には不純物として、2,4′体、
トリ体等のスルホン類とその他のスルホン酸類等
が含まれており、これからスルホン酸類等を除い
た4,4′体粗製品中の4,4′体の純度は通常70〜
80重量%程度である。 また、2,4′体の副生を抑制し、純度の高い
4,4′体を得る方法が開発されている。例えば脱
水反応により生成する4,4′体を析出せしめつつ
副生物の2,4′体を4,4′体に異性化させること
により、高純度4,4′体を収得する方法(特公昭
55−8972号)が提案されている。この場合の反応
生成物からスルホン酸類等を除いた4,4′体粗製
品中の4,4′体の純度は、通常90〜95重量%程度
である。然るに、前記各種用途のための4,4′体
の純度は。近年の樹脂に対する高品質化の要求等
のため、97重量%程度以上であることが要望され
るに至つている。従つて、前者の方法により製造
したものは更に精製することが必要であり、後者
の方法により製造したものも更に精製することが
望ましい。 4,4′体の精製法としては、例えばo−ジクロ
ルベンゼン−フエノール(特公昭51−36264号)、
o−ジクロルベンゼン−酢酸(特公昭57−48152
号)、o−ジクロルベンゼン−酢酸エチル(特公
昭57−48153号)、o−ジクロルベンゼン−アルコ
ール(特公昭58−2234号)等の各種混合有機溶剤
を用いて処理する方法が提案されている。しかし
ながら、これらの方法には、いずれも有機溶剤を
用いるため、取扱いが不便で作業衛生上の危険が
あり、又環境を汚染するという問題がある。 また、有機溶剤を用いない精製法としては、従
来から、水酸化ナトリウム等のアルカリ水溶液に
4,4′体粗製品を溶解した後、活性炭処理し、次
いで中和量以上の硫酸等の酸を加えて4,4′体を
析出させる方法が行なわれている。この方法は、
4,4′体が水に難溶性であるが、塩基性物質の水
溶液にはモノ又はジ金属塩等となつて容易に溶解
する性質を利用するものである。しかしながら、
この方法では、スルホン酸類は除去できるものの
2,4′体、トリ体等のスルホン類は殆んど除去で
きず、後記比較例に示すように精製品の純度が不
充分であり、前記要望には到底応え得ない。 発明が解決しようとする問題点 本発明の目的は、有機溶剤を用いることなく、
しかも高い精製収率(精製前の4,4′体に対する
収率)で且つ高純度の4,4′体を得るための精製
中間体として有用であり、前記要望に充分に応え
得る高純度4,4′体モノ金属塩の新規な製造方法
を提供することにある。 問題点を解決するための手段 本発明者は、上記目的を達成するべく鋭意研究
した結果、4,4′体粗製品を塩基性物質の水溶液
に溶解処理した後塩析するときには通常90%程度
以上という高収率で且つ98重量%程度以上という
高純度の4,4′体のモノ金属塩が析出するという
ユニークな事実を発見し、更にこれを酸処理する
ことにより通常85%程度以上という高い精製収率
で且つ99重量%程度以上という高純度の4,4′体
が得られることを見出した。この様に4,4′体が
特定条件下で高純度のモノ金属塩として塩析でき
るという事実は、4,4′体のモノ乃至ジ金属塩が
水に易溶性であるという常識を利用している当業
者にとつて全く予期し得ないことである。本発明
は、かかる新知見に基づいて完成されたものであ
る。 即ち本発明は、4,4′体粗製品を、塩基性物質
の水溶液に溶解処理した後塩析して4,4′体のモ
ノ金属塩を析出、分離することを特徴とする4,
4′体モノ金属塩の製造方法に係る。 本明細書においては、モノ金属塩とは、モノア
ルカリ金属塩、モノ1/2アルカリ土類金属塩等
を意味する。 本発明方法は、種々の4,4′体合成反応生成
物、該反応生成物からスルホン酸類等を除いたも
の及び4,4′体市販品を含めたいかなる純度の
4,4′体粗製品にも適用できる。 本発明において、4,4′体粗製品を、まず塩基
性物質の水溶液に、通常攪拌下に溶解処理する。
塩基性物質としては、ナトリウム、カリウム等の
アルカリ金属、カルシウム、マグネシウム等のア
ルカリ土類金属等の水酸化物、炭酸塩等を好まし
く使用できる。特に好ましいのは、水酸化ナトリ
ウム、炭酸ナトリウム等である。塩基性物質の使
用量は、スルホン酸類等の強酸分の中和量に加え
て、4,4′体、2,4′体、トリ体等のスルホン類
1モル当り1当量程度以上2当量程度以下とする
のが適当である。この範囲より少ない場合は、
4,4′体のモノ金属塩の塩析時に遊離の4,4′体
が混入して結晶形が悪くなり不純物の除去効果が
低下する傾向にあるので好ましくない。またこの
範囲より多い場合で且つそのまま塩析剤を加える
ことは、塩析されない4,4′体のジ金属塩が多量
に生成して収率が低下する傾向にあるので好まし
くない。但し、塩基性物質を4,4′体等のスルホ
ン類1モル当り2当量を越えて使用すること自体
は、何ら差し支えなく、本発明の有利な実施態様
の一つである。即ち、塩基性物質を2当量を越え
て過剰に使用して塩析されない4,4′体のジ金属
塩を多く生成させた溶解状態とすることにより、
必要ならば活性炭処理等を好適に行なうことがで
き、次いで酸を加えてジ金属塩をモノ金属塩に変
換すると同時に塩析剤を生成させ、必要に応じて
更に塩析剤を加えてモノ金属塩を塩析することが
できる。 上記の4,4′体粗製品の溶解処理においては、
処理液は、塩基性物質や水の使用量に対応して溶
液乃至懸濁状態を呈する。懸濁状態の場合は、概
して液相部分は4,4′体モノ金属塩と少量の4,
4′体ジ金属塩が溶解し、固相部分は一旦溶解後過
飽和となつて析出した4,4′体モノ金属塩を主体
とする状態であり、その後の塩析により液相部分
から4,4′体モノ金属塩が更に析出し結晶が成長
していくものと考えられる。 溶解処理の際の水の使用量は、広い範囲から選
択できるが、4,4′体粗製品に対して通常1.8〜
8.0重量部程度とするのが適当である。この範囲
よりも水量が少ないと固相部分の多い懸濁状態を
呈して流動性が乏しくなり攪拌が困難になる傾向
にあり、又この範囲よりも水量が多いと精製収率
が低下する傾向にあるので好ましくない。特に好
ましい水量は、4,4′体粗製品に対して1.3〜3.0
重量倍程度である。 また、溶解処理の際の温度は、特に限定されな
いが、40℃〜沸点程度とするのが4,4′体のモノ
金属塩の生成速度を大きくできる点で有利であ
る。 次に、上記で4,4′体粗製品を処理した溶液又
は懸濁液を、通常攪拌下に塩析して4,4′体のモ
ノ金属塩を析出させる。これにより、通常純度98
重量%程度以上という高純度の4,4′体モノ金属
塩が通常原料粗製品中の4,4′体に対して87%以
上という高い収率で析出してくる。この事実は、
本発明者により初めて発見されたものである。 塩析は、塩析剤を添加するか、前記塩基性物質
を過剰に加え、これに塩酸、硫酸等の酸を加えて
塩析剤を生成させるか、又はこれらの方法を併用
することにより行なわれる。塩析剤としては、ナ
トリウム、カリウム等のアルカリ金属、カルシウ
ム、マグネシウム等のアルカリ土類金属等の塩化
物、硫酸塩等を好ましく使用できる。また、塩析
剤の使用量は、広い範囲から選択でき、通常濃度
として2重量%以上飽和濃度以下となる量とする
のが適当である。この範囲より少ないと塩析効果
が低く収率が低下するので好ましくない。また、
飽和濃度以上では塩析剤の結晶が析出するので好
ましくない。塩析剤の好ましい使用量は、通常4
〜15重量%程度となる量である。 塩析剤投入の際の温度は、特に限定されない
が、40℃〜沸点程度とするのが、4,4′体モノ金
属塩の結晶形を良くして収率、純度を向上させる
点から有利である。塩析剤投入後は、その温度で
0.2〜12時間程度熟成させても良い。 次いで、析出した4,4′体モノ金属塩を過等
により分離し、必要に応じて適宜洗浄して高純度
の4,4′体モノ金属塩を得る。 本発明により製造される4,4′体モノ金属塩
は、高純度4,4′体を得るための精製中間体とし
て極めて有用であり、通常は、これを酸処理して
遊離の4,4′体を得る。酸処理は、常法に従つて
行なえば良く、4,4′体モノ金属塩を水又はアル
カリ水溶液に溶解し、必要に応じて活性炭処理を
行つた後、硫酸、塩酸等の酸を添加してPHを3〜
6程度とし、析出する4,4′体を過等により分
離することにより、ほぼ定量的に行なわれる。 かくして、4,4′体を高い精製収率且つ高純度
で精製することができる。 また、本発明により得られる高純度4,4′体モ
ノ金属塩は、用途によつては、そのまま工業原料
として使用することもできる。 発明の効果 本発明法により得られる高純度4,4′体モノ金
属塩を4,4′体精製中間体として用いることによ
り、下記の如き格別顕著な効果が奏される。 (1) 有機溶剤を用いないので、取扱いが容易で、
作業衛生上、環境上の問題がない。 (2) 通常、85%以上という高い精製収率で、99重
量%以上という高純度の4,4′体を収得でき、
前記業界の要望に充分に応え得るものである。 (3) 従来法に比して、少量の液量で多量の精製が
効率的に実施できる。また、設備をコンパクト
にでき、作業性が良い。 実施例 以下、参考例、実施例及び比較例を挙げて本発
明を更に具体的に説明する。 参考例 1 特公昭55−8972号の方法により、4,4′体粗製
品を製造した。 即ち、フエノール290g、98重量%硫酸146g及
びo−ジクロルベンゼン(ODCB)150gの混合
物を、攪拌下加熱した。150℃付近より反応液が
沸騰し、ODCBと共に反応生成水が留出し始め
た。留出液を凝縮し、ODCB相を連続的に反応系
内に戻し、水相の液量が52mlに達した時点より反
応温度を175〜185℃に保ち、減圧度を調整しなが
ら生成水及びフエノールを少量含有するODCBを
4時間を要して反応物が乾固するまで、蒸留回収
した。 ここで得た反応乾固物の高速液体クロマトグラ
フイーによる分析結果は、4,4′体84.6重量%、
2,4′体2.0重量%、トリ体4.5重量%及びその他
のスルホン酸類等が8.9重量%であつた。 実施例 1 参考例1で得た4,4′体粗製品である反応乾固
物100gを、水155gと水酸化ナトリウム18.1g(スル
ホン酸分の中和に必要な量と4,4′体、2,4′体
及びトリ体のスルホン類の総和に対して1.2倍当
量の量との合計に相当する。)に加えて、攪拌下
昇温し、95℃とした。液は完全には溶解せず懸濁
状態であつた。 次に、食塩10gを加え、同温度で30分間保持し
て熟成した後冷却した。50℃1時間保温した後、
析出物を取し、5重量%食塩水50mlで洗浄して
4,4′体モノナトリウム塩84.0g(精製収率91.3%)
を得た。 得られた4,4′体モノナトリウム塩を塩酸処理
後、高速液体クロマトグラフイーにより分析した
結果を第1表に示す。 上記で得られた4,4′体モノナトリウム塩を水
900mlに溶解し、90〜95℃の温度で78重量%硫酸
を加え、PH4.0迄中和し4,4′体を析出させた。
40℃まで冷却した後、取、乾燥して、4,4′体
精製品76.6gを得た。精製収率は90.4%(対 原
料中の4,4′体)であつた。 高速液体クロマトグラフイーによる分析結果
は、第1表の通りであつた。 実施例 2 実施例1において塩析剤である食塩10gに代え
て無水硫酸ナトリウム15gを用いた他は実施例1
と同様に塩析処理して4,4′体モノナトリウム塩
83.2g(精製収率90.4%)を得、更に同様に硫酸処
理して4,4′体精製品75.9gを得た。 精製収率は、89.5%であり、高速液体クロマト
グラフイーにより分析した結果は、第1表の通り
であつた。 実施例 3 参考例1で得た4,4′体粗製品たる反応乾固物
100gを、水280gと水酸化ナトリウム31.6g(スルホ
ン酸分の中和に必要な量と4,4′体等のスルホン
類の総和、に対して2.1倍当量の量との合計に相
当する。)に加えて、攪拌下昇温し、95℃とした。
液は完全に溶解していた。 次に、78重量%硫酸24.1gを徐々に加えた後、
冷却し50℃で1時間保温した後、析出結晶を取
し、5重量%硫酸ナトリウム水で洗浄して4,
4′体モノナトリウム塩81.0g(精製収率88.0%)を
得た。 得られた4,4′体モノナトリウム塩の高速液体
クロマトグラフイーによる分析の結果、その組成
比は、第1表の通りであつた。 上記で得られた4,4′体モノナトリウム塩を、
実施例1と同様に硫酸処理したところ、4,4′体
精製品73.9gを得た。精製収率は87.3%であり、
高速液体クロマトグラフイーによる分析結果は、
第1表の通りであつた。 実施例 4 市販の4,4′体粗製品の組成を高速液体クロマ
トグラフイーにより分析したところ4,4′体、
2,4′体、トリ体が、それぞれ82.6重量%。14.0
重量%。3.4重量%であつた。 この粗製品100gを、水160gと水酸化ナトリウ
ム33.2g(4,4′体等のスルホン類の総和に対して
2.1倍当量)に加え、攪拌下97℃に昇温した。液
は完全に溶解せず懸濁状態であつた。 次に、78重量%硫酸25.1gを徐々に加えた後、
冷却し50℃で1時間保温した後、析出結晶を取
し、5重量%硫酸ナトリウム水で洗浄して、4,
4′体モノナトリウム塩80.4g(精製収率87.4%)を
得た。 得られた4,4′体モノナトリウム塩の高速液体
クロマトグラフイーによる分析の結果、その組成
比は、第1表の通りであつた。 上記で得られた4,4′体モノナトリウム塩を、
実施例1と同様に処理したところ、4,4′体精製
品71.5gを得た。精製収率は85.8重量%であり、
高速液体クロマトグラフイーによる分析の結果
は、第1表の通りであつた。
INDUSTRIAL APPLICATION FIELD OF THE INVENTION The present invention relates to a novel method for producing high-purity 4,4'-dihydroxydiphenylsulfone monometallic salts in high yields from crude 4,4'-dihydroxydiphenylsulfone products. Conventional technology 4,4'-dihydroxydiphenyl sulfone (hereinafter referred to as 4,4' body) has excellent heat resistance, oxidation resistance, light stability, etc., so it has recently been used in polyester resins, epoxy resins, and polycarbonates. It has come to be widely used in the field of polymer chemical industry, such as resins and polyethersulfone resins. In this case, synthesis is performed using 4,4'-form as a raw material containing impurities such as 2,4'-dihydroxydiphenylsulfone (hereinafter referred to as 2,4'-form) and trihydroxytriphenyldisulfone (hereinafter referred to as "tri-form"). The resulting polymer product tends to have a lower molecular weight and lower mechanical properties, and this tendency becomes more pronounced as the amount of impurities such as 2,4' and tri-isomers increases. Therefore, 2,
There is a demand for the supply of highly pure 4,4'-isomers from which impurities such as 4'-isomers and tri-isomers have been removed as much as possible. In addition, the 4,4′ body is a coupler raw material for color photography,
It is also useful as a color developer for heat-sensitive recording paper, and in this case as well, high purity is desirable. Industrially, the 4,4'-isomer is mainly produced by a dehydration reaction between phenol and a sulfonating agent such as sulfuric acid, and the reaction product contains impurities such as the 2,4'-isomer,
Contains sulfones such as tri-isomers and other sulfonic acids, etc., and the purity of the 4,4'-isomer in the 4,4'-isomer crude product after removing sulfonic acids, etc. is usually 70~70~
It is about 80% by weight. In addition, a method has been developed to suppress the by-product of 2,4'-isomer and obtain highly pure 4,4'-isomer. For example, a method of obtaining highly pure 4,4' isomer by precipitating the 4,4' isomer produced by a dehydration reaction and isomerizing the by-product 2,4' isomer into 4,4' isomer.
No. 55-8972) has been proposed. In this case, the purity of the 4,4' product in the crude 4,4' product obtained by removing sulfonic acids and the like from the reaction product is usually about 90 to 95% by weight. However, the purity of the 4,4' form for the various uses mentioned above. Due to recent demands for higher quality resins, a content of about 97% by weight or more has come to be desired. Therefore, it is necessary to further purify those produced by the former method, and it is desirable to further refine those produced by the latter method. As a method for purifying the 4,4'-isomer, for example, o-dichlorobenzene-phenol (Japanese Patent Publication No. 51-36264),
o-dichlorobenzene-acetic acid (Special Publication No. 57-48152
Treatment methods using various mixed organic solvents such as o-dichlorobenzene-ethyl acetate (Japanese Patent Publication No. 57-48153), and o-dichlorobenzene-alcohol (Japanese Patent Publication No. 58-2234) have been proposed. ing. However, since all of these methods use organic solvents, they are inconvenient to handle, pose a health hazard, and pollute the environment. In addition, conventional purification methods that do not use organic solvents include dissolving the 4,4' crude product in an alkaline aqueous solution such as sodium hydroxide, treating it with activated carbon, and then adding an acid such as sulfuric acid in an amount greater than the neutralizing amount. In addition, a method of precipitating the 4,4' isomer has been used. This method is
The 4,4' form is poorly soluble in water, but it takes advantage of the property that it easily dissolves in aqueous solutions of basic substances in the form of mono- or di-metal salts. however,
Although this method can remove sulfonic acids, it cannot remove most of the 2,4'- and tri-sulfones, and as shown in the comparative example below, the purity of the purified product is insufficient to meet the above requirements. cannot be answered at all. Problems to be Solved by the Invention The purpose of the present invention is to solve the problem without using an organic solvent.
In addition, it is useful as a purification intermediate for obtaining the 4,4'-isomer with a high purification yield (yield relative to the 4,4'-isomer before purification) and high purity, and can sufficiently meet the above-mentioned needs. , 4' monometallic salts. Means for Solving the Problems As a result of intensive research to achieve the above object, the present inventor has found that when a crude 4,4' product is dissolved in an aqueous solution of a basic substance and then salted out, the percentage is usually about 90%. We discovered the unique fact that a 4,4' monometallic salt can be precipitated with a high yield of 98% by weight or higher, and by further treating it with an acid, a purity of 85% or higher is usually obtained. It has been found that the 4,4' isomer can be obtained with a high purification yield and a high purity of about 99% by weight or more. The fact that the 4,4'-isomer can be salted out as a highly pure monometallic salt under specific conditions is based on the common knowledge that 4,4'-isomer mono- and dimetallic salts are easily soluble in water. This is completely unexpected for those skilled in the art. The present invention was completed based on this new knowledge. That is, the present invention is characterized in that the 4,4' crude product is dissolved in an aqueous solution of a basic substance and then salted out to precipitate and separate the 4,4' monometallic salt.
This invention relates to a method for producing a 4' monometallic salt. As used herein, monometallic salts refer to monoalkali metal salts, mono1/2 alkaline earth metal salts, and the like. The method of the present invention can be applied to various 4,4' synthesis reaction products, 4,4' crude products of any purity, including products from which sulfonic acids have been removed, and commercially available 4,4' products. It can also be applied to In the present invention, the crude 4,4' product is first dissolved in an aqueous solution of a basic substance, usually under stirring.
As the basic substance, hydroxides and carbonates of alkali metals such as sodium and potassium, alkaline earth metals such as calcium and magnesium, etc. can be preferably used. Particularly preferred are sodium hydroxide, sodium carbonate, and the like. The amount of the basic substance to be used is approximately 1 equivalent or more and approximately 2 equivalents per mole of sulfones such as 4,4', 2,4', and tri-isomers, in addition to the neutralizing amount of strong acids such as sulfonic acids. The following is appropriate. If it is less than this range,
This is not preferable since free 4,4' is mixed in during salting out of a monometallic salt of 4,4', which tends to deteriorate the crystal shape and reduce the impurity removal effect. Further, if the amount exceeds this range and the salting-out agent is added as is, a large amount of 4,4' dimetal salts that are not salted out tend to be produced, resulting in a decrease in yield, which is not preferable. However, the use of the basic substance in an amount exceeding 2 equivalents per mole of sulfones such as 4,4' sulfones does not pose any problem and is an advantageous embodiment of the present invention. That is, by using an excess of more than 2 equivalents of a basic substance to create a dissolved state in which a large amount of 4,4' dimetal salt that is not salted out is produced,
If necessary, activated carbon treatment etc. can be suitably carried out, and then an acid is added to convert the dimetal salt into a monometallic salt, at the same time a salting-out agent is generated, and if necessary, a salting-out agent is further added to convert the dimetallic salt into a monometallic salt. Salt can be salted out. In the above-mentioned dissolution treatment of the 4,4′ crude product,
The processing liquid exhibits a solution or suspension state depending on the amount of basic substance and water used. In a suspended state, the liquid phase generally consists of a 4,4' monometallic salt and a small amount of 4,4' monometallic salt.
The 4' dimetal salt is dissolved, and the solid phase is mainly composed of the 4,4' monometal salt that becomes supersaturated and precipitates after dissolution, and the subsequent salting out removes the 4,4' dimetal salt from the liquid phase. It is thought that the 4′ monometallic salt further precipitates and the crystals grow. The amount of water used during dissolution treatment can be selected from a wide range, but it is usually 1.8 to
Approximately 8.0 parts by weight is appropriate. If the amount of water is less than this range, a suspension state with a large amount of solid phase will occur, resulting in poor fluidity and stirring will tend to become difficult, and if the amount of water is more than this range, the purification yield will tend to decrease. I don't like it because it is. A particularly preferable amount of water is 1.3 to 3.0 for the 4,4′ crude product.
It is about twice the weight. Further, the temperature during the dissolution treatment is not particularly limited, but it is advantageous to set it to about 40° C. to the boiling point in that the production rate of the 4,4′ monometallic salt can be increased. Next, the solution or suspension obtained by treating the crude 4,4' product as described above is salted out, usually with stirring, to precipitate the monometallic salt of the 4,4' product. This typically results in a purity of 98
The 4,4' monometallic salt with a high purity of about % by weight or more is usually precipitated in a high yield of 87% or more based on the 4,4' monometal salt in the crude raw material. This fact is
This was discovered for the first time by the present inventor. Salting out is carried out by adding a salting out agent, adding an excess of the basic substance and adding an acid such as hydrochloric acid or sulfuric acid to generate a salting out agent, or using a combination of these methods. It will be done. As the salting-out agent, chlorides and sulfates of alkali metals such as sodium and potassium, alkaline earth metals such as calcium and magnesium, etc. can be preferably used. Further, the amount of the salting-out agent to be used can be selected from a wide range, and it is usually appropriate to set the amount to be at least 2% by weight and at most the saturation concentration. If the amount is less than this range, the salting-out effect will be low and the yield will decrease, which is not preferable. Also,
If the concentration exceeds the saturation concentration, crystals of the salting-out agent will precipitate, which is not preferable. The preferred usage amount of the salting-out agent is usually 4
The amount is approximately 15% by weight. The temperature when adding the salting-out agent is not particularly limited, but it is advantageous to set it to about 40°C to the boiling point in order to improve the crystal form of the 4,4' monometallic salt and improve the yield and purity. It is. After adding salting out agent, at that temperature
It may be aged for about 0.2 to 12 hours. Next, the precipitated 4,4' monometallic salt is separated by filtration and, if necessary, washed appropriately to obtain a highly purified 4,4' monometallic salt. The 4,4' monometallic salt produced by the present invention is extremely useful as a purification intermediate for obtaining highly purified 4,4' monometallic salts, and is usually acid-treated to form free 4,4' monometallic salts. ' Get a body. Acid treatment can be carried out according to a conventional method, and the 4,4' monometal salt is dissolved in water or an alkaline aqueous solution, treated with activated carbon if necessary, and then an acid such as sulfuric acid or hydrochloric acid is added. and pH 3~
6, and the precipitated 4,4' isomer is separated by filtration, etc., and the result is almost quantitative. In this way, the 4,4'-isomer can be purified with high purification yield and high purity. Further, the highly purified 4,4' monometallic salt obtained by the present invention can be used as it is as an industrial raw material depending on the application. Effects of the Invention By using the highly purified 4,4' monometallic salt obtained by the method of the present invention as a 4,4' monometallic intermediate, the following particularly remarkable effects can be achieved. (1) Easy to handle because no organic solvent is used.
There are no occupational hygiene or environmental problems. (2) Usually, the 4,4′ isomer can be obtained with a high purification yield of 85% or more and a high purity of 99% by weight or more.
This can fully meet the demands of the industry. (3) Compared to conventional methods, a large amount of purification can be efficiently carried out using a small amount of liquid. Additionally, the equipment can be made compact and workability is good. EXAMPLES Hereinafter, the present invention will be explained in more detail with reference to reference examples, examples, and comparative examples. Reference Example 1 A 4,4' crude product was produced by the method described in Japanese Patent Publication No. 55-8972. That is, a mixture of 290 g of phenol, 146 g of 98% by weight sulfuric acid, and 150 g of o-dichlorobenzene (ODCB) was heated with stirring. The reaction solution boiled around 150°C, and reaction product water began to distill out along with ODCB. The distillate is condensed, the ODCB phase is continuously returned to the reaction system, and from the point when the liquid volume of the aqueous phase reaches 52 ml, the reaction temperature is maintained at 175 to 185°C, and the produced water and The ODCB containing a small amount of phenol was recovered by distillation over a period of 4 hours until the reaction product was dried to dryness. The analysis results of the dried reaction product obtained here by high performance liquid chromatography showed that 84.6% by weight of the 4,4′ isomer;
2.0% by weight of 2,4'-isomer, 4.5% by weight of tri-isomer, and 8.9% by weight of other sulfonic acids. Example 1 100 g of the reaction dry product, which is the crude 4,4' product obtained in Reference Example 1, was mixed with 155 g of water and 18.1 g of sodium hydroxide (the amount necessary for neutralizing the sulfonic acid content and the 4,4' product). , 1.2 times the equivalent of the total amount of 2,4'- and tri-sulfones), and the temperature was raised to 95° C. with stirring. The liquid was not completely dissolved and remained in a suspended state. Next, 10 g of common salt was added, and the mixture was kept at the same temperature for 30 minutes to age and then cooled. After keeping warm at 50℃ for 1 hour,
The precipitate was collected and washed with 50 ml of 5% brine to obtain 84.0 g of 4,4' monosodium salt (purification yield 91.3%).
I got it. The obtained 4,4' monosodium salt was treated with hydrochloric acid and analyzed by high performance liquid chromatography. The results are shown in Table 1. The 4,4′ monosodium salt obtained above was dissolved in water.
The solution was dissolved in 900 ml, and 78% by weight sulfuric acid was added at a temperature of 90 to 95°C to neutralize the pH to 4.0 to precipitate the 4,4' isomer.
After cooling to 40°C, it was taken and dried to obtain 76.6 g of a purified 4,4' product. The purification yield was 90.4% (based on the 4,4' isomer in the raw material). The analysis results by high performance liquid chromatography were as shown in Table 1. Example 2 Example 1 except that 15 g of anhydrous sodium sulfate was used in place of 10 g of common salt as a salting-out agent in Example 1.
Salting out in the same manner as 4,4′ monosodium salt
83.2g (purification yield: 90.4%) was obtained, which was further treated with sulfuric acid in the same manner to obtain 75.9g of a 4,4' purified product. The purification yield was 89.5%, and the results of analysis by high performance liquid chromatography were as shown in Table 1. Example 3 Reaction dried product as 4,4' crude product obtained in Reference Example 1
100g corresponds to the sum of 280g of water and 31.6g of sodium hydroxide (an amount equivalent to 2.1 times the amount required for neutralizing the sulfonic acid component and the total amount of sulfones such as 4,4' bodies). ), and the temperature was raised to 95°C while stirring.
The liquid was completely dissolved. Next, after gradually adding 24.1 g of 78 wt% sulfuric acid,
After cooling and keeping at 50°C for 1 hour, the precipitated crystals were collected and washed with 5% by weight sodium sulfate water.
81.0 g (purification yield: 88.0%) of 4' monosodium salt was obtained. As a result of analysis of the obtained 4,4' monosodium salt by high performance liquid chromatography, the composition ratio was as shown in Table 1. The 4,4' monosodium salt obtained above was
When treated with sulfuric acid in the same manner as in Example 1, 73.9 g of a purified 4,4' product was obtained. The purification yield is 87.3%,
The analysis results by high performance liquid chromatography are
It was as shown in Table 1. Example 4 The composition of a commercially available crude product of 4,4' body was analyzed by high performance liquid chromatography, and it was found that 4,4' body,
2,4' and tri-isomers each account for 82.6% by weight. 14.0
weight%. It was 3.4% by weight. 100g of this crude product was mixed with 160g of water and 33.2g of sodium hydroxide (based on the total amount of sulfones such as 4,4'-sulfones).
2.1 times equivalent) and the temperature was raised to 97°C while stirring. The liquid was not completely dissolved and remained in a suspended state. Next, after gradually adding 25.1 g of 78 wt% sulfuric acid,
After cooling and keeping at 50°C for 1 hour, the precipitated crystals were collected and washed with 5% by weight sodium sulfate water.
80.4 g (purification yield: 87.4%) of 4' monosodium salt was obtained. As a result of analysis of the obtained 4,4' monosodium salt by high performance liquid chromatography, its composition ratio was as shown in Table 1. The 4,4' monosodium salt obtained above was
When treated in the same manner as in Example 1, 71.5 g of a purified 4,4' product was obtained. The purification yield is 85.8% by weight,
The results of analysis by high performance liquid chromatography are shown in Table 1.

【表】 比較例 1 参考例1で得た4,4′体粗製品100g、水酸化ナ
トリウム31.6g及び水280gを攪拌下昇温溶解し、
95℃にて78重量%硫酸48.0gを加え、PH=4とし
た後、冷却し50℃で1時間保温した後、別、乾
燥し4,4′体89.9gを得た。収率は99.3%であり、
高速液体クロマトグラフイーによる分析結果は
4,4′体93.4重量%、2,4′体1.7重量%、トリ体
4.9重量%であつた。
[Table] Comparative Example 1 100 g of the 4,4′ crude product obtained in Reference Example 1, 31.6 g of sodium hydroxide, and 280 g of water were dissolved at elevated temperature with stirring.
After adding 48.0 g of 78% by weight sulfuric acid at 95°C to adjust the pH to 4, the mixture was cooled, kept at 50°C for 1 hour, and dried separately to obtain 89.9 g of 4,4' compound. The yield is 99.3%,
Analysis results by high-performance liquid chromatography showed 93.4% by weight of 4,4′ form, 1.7% by weight of 2,4′ form, and 1.7% by weight of tri form.
It was 4.9% by weight.

Claims (1)

【特許請求の範囲】 4,4′−ジヒドロキシジフエニルスルホン粗
製品を、塩基性物質の水溶液に溶解処理した後塩
析して4,4′−ジヒドロキシジフエニルスルホン
のモノ金属塩を析出、分離することを特徴とする
4,4′−ジヒドロキシジフエニルスルホンモノ金
属塩の製造法。
[Claims] A crude product of 4,4'-dihydroxydiphenylsulfone is dissolved in an aqueous solution of a basic substance and then salted out to precipitate and separate a monometallic salt of 4,4'-dihydroxydiphenylsulfone. A method for producing 4,4'-dihydroxydiphenylsulfone monometallic salt, characterized in that:
JP20843587A 1987-08-21 1987-08-21 Production of 4,4'-dihydroxydiphenylsulfone monometallic salt Granted JPS6450856A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP20843587A JPS6450856A (en) 1987-08-21 1987-08-21 Production of 4,4'-dihydroxydiphenylsulfone monometallic salt
DE3890647A DE3890647C2 (en) 1987-08-21 1988-08-17 Process for the purification of crude 4,4'-dihydroxydiphenyl sulfone
PCT/JP1988/000813 WO1989001469A1 (en) 1987-08-21 1988-08-17 Process for purifying 4,4'-dihydroxydiphenyl sulfone
GB8908173A GB2216125B (en) 1987-08-21 1988-08-17 Process for purifying 4,4'-dihydroxydiphenylsulfone
DE19883890647 DE3890647T1 (en) 1987-08-21 1988-08-17 METHOD FOR PURIFYING 4,4'-DIHYDROXYDIPHENYL SULPHONE
US07/362,411 US5097074A (en) 1987-08-21 1988-08-17 Process for purifying 4,4'-dihydroxydiphenylsulfone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20843587A JPS6450856A (en) 1987-08-21 1987-08-21 Production of 4,4'-dihydroxydiphenylsulfone monometallic salt

Publications (2)

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JPS6450856A JPS6450856A (en) 1989-02-27
JPH05383B2 true JPH05383B2 (en) 1993-01-05

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