JPS5934170B2 - ジフェニル炭酸エステルの製法 - Google Patents

ジフェニル炭酸エステルの製法

Info

Publication number: JPS5934170B2
Authority: JP; Japan
Prior art keywords: carbonate; diphenyl carbonate; production method; carbonate ester; phenol
Prior art date: 1974-06-25
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

Application number

JP56023198A

Other languages

English (en)

Japanese (ja)

Other versions

JPS56123948A (en

Inventor

ガブリエロ・イルミナ−チ

ユ−ゴ・ロマノ

レナ−ト・テセイ

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.)

Anic SpA

Original Assignee

Anic SpA

Priority date (The priority date 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 date listed.)

1974-06-25

Filing date

1981-02-20

Publication date

1984-08-21

1981-02-20 Application filed by Anic SpA filed Critical Anic SpA

1981-09-29 Publication of JPS56123948A publication Critical patent/JPS56123948A/ja

1984-08-21 Publication of JPS5934170B2 publication Critical patent/JPS5934170B2/ja

Status Expired legal-status Critical Current

Links

-1 diphenyl carbonate ester Chemical class 0.000 title claims description 5
238000004519 manufacturing process Methods 0.000 title claims description 5
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 7
ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 claims description 6
239000003054 catalyst Substances 0.000 claims description 4
125000005910 alkyl carbonate group Chemical group 0.000 claims description 3
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
238000006243 chemical reaction Methods 0.000 description 9
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
125000003118 aryl group Chemical group 0.000 description 6
IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 4
238000000034 method Methods 0.000 description 4
229940049953 phenylacetate Drugs 0.000 description 4
WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 4
239000010936 titanium Substances 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
YCNSGSUGQPDYTK-UHFFFAOYSA-N ethyl phenyl carbonate Chemical compound CCOC(=O)OC1=CC=CC=C1 YCNSGSUGQPDYTK-UHFFFAOYSA-N 0.000 description 3
239000002994 raw material Substances 0.000 description 3
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
239000002841 Lewis acid Substances 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
125000004104 aryloxy group Chemical group 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
238000004821 distillation Methods 0.000 description 2
150000007517 lewis acids Chemical class 0.000 description 2
238000000926 separation method Methods 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
LRMHFDNWKCSEQU-UHFFFAOYSA-N ethoxyethane;phenol Chemical compound CCOCC.OC1=CC=CC=C1 LRMHFDNWKCSEQU-UHFFFAOYSA-N 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 1
239000002184 metal Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
ZEIWWVGGEOHESL-UHFFFAOYSA-N methanol;titanium Chemical compound [Ti].OC.OC.OC.OC ZEIWWVGGEOHESL-UHFFFAOYSA-N 0.000 description 1
239000000203 mixture Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
150000003623 transition metal compounds Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/06—Preparation of esters of carbonic or haloformic acids from organic carbonates

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Polyesters Or Polycarbonates (AREA)

JP56023198A 1974-06-25 1981-02-20 ジフェニル炭酸エステルの製法 Expired JPS5934170B2 (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
IT24392A/74		1974-06-25
IT24392/74A IT1015377B (it)	1974-06-25	1974-06-25	Processo per la preparazione di carbonati aromatici
IT20191A/75		1975-02-12

Publications (2)

Publication Number	Publication Date
JPS56123948A JPS56123948A (en)	1981-09-29
JPS5934170B2 true JPS5934170B2 (ja)	1984-08-21

Family

ID=11213360

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
JP56023198A Expired JPS5934170B2 (ja)	1974-06-25	1981-02-20	ジフェニル炭酸エステルの製法
JP56023199A Expired JPS5934171B2 (ja)	1974-06-25	1981-02-20	ビスフェノ−ルａポリアルキル炭酸エステルの製法

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
JP56023199A Expired JPS5934171B2 (ja)	1974-06-25	1981-02-20	ビスフェノ−ルａポリアルキル炭酸エステルの製法

Country Status (7)

Country	Link
JP (2)	JPS5934170B2 (fr)
BE (1)	BE830364A (fr)
HU (1)	HU171825B (fr)
IN (1)	IN143867B (fr)
IT (1)	IT1015377B (fr)
MW (1)	MW3575A1 (fr)
ZA (1)	ZA753587B (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4452968A (en) *	1981-11-30	1984-06-05	General Electric Company	Synthesis of polycarbonate from dialkyl carbonate and bisphenol diester
JP2733035B2 (ja) *	1994-05-31	1998-03-30	株式会社日本触媒	炭酸エステルの製造方法
JP2733036B2 (ja) *	1994-07-05	1998-03-30	株式会社日本触媒	炭酸エステルの製造方法
JP2922848B2 (ja) *	1996-06-14	1999-07-26	株式会社日本触媒	芳香族炭酸エステルの製造方法
JP5014787B2 (ja)	2004-06-17	2012-08-29	旭化成ケミカルズ株式会社	芳香族カーボネートの製造方法
BRPI0513251A (pt)	2004-07-13	2008-05-13	Asahi Kasei Chemicals Corp	processo para a produção de um carbonato aromático, e, carbonato aromático
WO2006006566A1 (fr)	2004-07-13	2006-01-19	Asahi Kasei Chemicals Corporation	Procédé industriel de fabrication de carbonate aromatique
CN100543006C (zh)	2004-07-14	2009-09-23	旭化成化学株式会社	芳香族碳酸酯类的工业制备方法
CN100532348C (zh)	2004-07-14	2009-08-26	旭化成化学株式会社	芳香族碳酸酯类的工业制备方法
BRPI0514564B1 (pt)	2004-08-25	2015-06-09	Asahi Kasei Chemicals Corp	Processo industrial para produção de carbonato de difenila de pureza elevada e aparelho para produzir carbonato de difenila de pureza elevada
KR100880141B1 (ko)	2004-09-03	2009-01-23	아사히 가세이 케미칼즈 가부시키가이샤	고순도 디아릴카보네이트의 공업적 제조 방법
CN100554241C (zh)	2004-09-17	2009-10-28	旭化成化学株式会社	醇类副产物的工业分离方法
JP4292214B2 (ja)	2004-10-14	2009-07-08	旭化成ケミカルズ株式会社	高純度ジアリールカーボネートの製造方法
TWI321561B (en)	2004-12-21	2010-03-11	Asahi Kasei Chemicals Corp	Method for producing aromatic carbonate
JP4195717B2 (ja)	2004-12-24	2008-12-10	旭化成ケミカルズ株式会社	芳香族カーボネートの製造方法
JP5589266B2 (ja) *	2008-06-09	2014-09-17	宇部興産株式会社	ポリ（アルキレンカーボネート）化合物の製造方法

1974
- 1974-06-25 IT IT24392/74A patent/IT1015377B/it active
1975
- 1975-06-03 ZA ZA00753587A patent/ZA753587B/xx unknown
- 1975-06-07 MW MW35/75A patent/MW3575A1/xx unknown
- 1975-06-16 IN IN1177/CAL/75A patent/IN143867B/en unknown
- 1975-06-18 BE BE157438A patent/BE830364A/fr not_active IP Right Cessation
- 1975-06-24 HU HU75SA00002809A patent/HU171825B/hu unknown
1981
- 1981-02-20 JP JP56023198A patent/JPS5934170B2/ja not_active Expired
- 1981-02-20 JP JP56023199A patent/JPS5934171B2/ja not_active Expired

Also Published As

Publication number	Publication date
IT1015377B (it)	1977-05-10
BE830364A (fr)	1975-10-16
JPS5934171B2 (ja)	1984-08-21
HU171825B (hu)	1978-03-28
MW3575A1 (en)	1976-10-13
IN143867B (fr)	1978-02-18
JPS56123949A (en)	1981-09-29
JPS56123948A (en)	1981-09-29
ZA753587B (en)	1976-05-26

Publication	Publication Date	Title
US4045464A (en)	1977-08-30	Process for the preparation of aromatic carbonates
US4182726A (en)	1980-01-08	Process for the preparation of aromatic carbonates
JPS5934170B2 (ja)	1984-08-21	ジフェニル炭酸エステルの製法
KR102605180B1 (ko)	2023-11-24	시클릭 카르보네이트를 제조하는 방법
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US6093857A (en)	2000-07-25	Preparation of cyclopentanols
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JPS63192731A (ja)	1988-08-10	β−アリールアルコールの製法
US2449447A (en)	1948-09-14	Preparation of ether esters
CN103539734B (zh)	2015-10-14	3-烯丙基喹啉的制备方法
AU640201B2 (en)	1993-08-19	Preparation of 2,2-dialkoxy cyclic orthoesters derived from lactones
SU466224A1 (ru)	1975-04-05	Способ получени производных 1,1ди-(фурил-2) -циклогексана
EP2325167A1 (fr)	2011-05-25	Procédé de fabrication d'un composé carbamate
JPS62263194A (ja)	1987-11-16	テトラアセチルアルブチンの製造法
KR20050010050A (ko)	2005-01-26	1,2,4-부탄트리올의 제조 방법
US3026349A (en)	1962-03-20	Production of trans-beta-styrylthioglycolic acid
US4031136A (en)	1977-06-21	Process for the preparation of trans, trans-muconic acid
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KR890002552B1 (ko)	1989-07-18	알콕시 니트로벤젠의 제조방법
JPH0469362A (ja)	1992-03-04	アセト酢酸ｌ―メンチルエステルの製造方法
JPH03106849A (ja)	1991-05-07	２‐エトキシメチレンアセト酢酸アルキルの製造方法
JPS6014014B2 (ja)	1985-04-11	炭酸エステルの製造方法
JPH03258768A (ja)	1991-11-19	１，３，５―パーヒドロトリアジン―２，４，６―トリチオン誘導体の製造方法