SU495824A3 - Способ получени незамещенных или замещенных пара-или мета-фенилендиаминов - Google Patents

Способ получени незамещенных или замещенных пара-или мета-фенилендиаминов

Info

Publication number: SU495824A3
Authority: SU; USSR - Soviet Union
Prior art keywords: meta; unsubstituted; phenylenediamine; obtaining; substituted para
Prior art date: 1972-04-01

Application number

SU1899019A

Other languages

English (en)

Russian (ru)

Inventor

Ценгель Ханс

Бергфельд Манфред

Original Assignee

Акцо Нв. (Фирма)

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.)

1972-04-01

Filing date

1973-03-30

Publication date

1975-12-15

1973-03-30 Application filed by Акцо Нв. (Фирма) filed Critical Акцо Нв. (Фирма)

1975-12-15 Application granted granted Critical

1975-12-15 Publication of SU495824A3 publication Critical patent/SU495824A3/ru

Links

238000000034 method Methods 0.000 title description 3
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical class NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 title 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical class NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 title 1
238000006243 chemical reaction Methods 0.000 description 8
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
229910000410 antimony oxide Inorganic materials 0.000 description 6
VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 6
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
239000003054 catalyst Substances 0.000 description 5
239000000047 product Substances 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
238000001816 cooling Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical class OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000203 mixture Substances 0.000 description 2
HZLCGUXUOFWCCN-UHFFFAOYSA-N 2-hydroxynonadecane-1,2,3-tricarboxylic acid Chemical compound CCCCCCCCCCCCCCCCC(C(O)=O)C(O)(C(O)=O)CC(O)=O HZLCGUXUOFWCCN-UHFFFAOYSA-N 0.000 description 1
UFMBOFGKHIXOTA-UHFFFAOYSA-N 2-methylterephthalic acid Chemical compound CC1=CC(C(O)=O)=CC=C1C(O)=O UFMBOFGKHIXOTA-UHFFFAOYSA-N 0.000 description 1
YTLWDDZIUHEODJ-UHFFFAOYSA-N 4-methylcyclohexa-1,5-diene-1,4-dicarboxylic acid Chemical compound OC(=O)C1(C)CC=C(C(O)=O)C=C1 YTLWDDZIUHEODJ-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
239000008896 Opium Substances 0.000 description 1
235000001484 Trigonella foenum graecum Nutrition 0.000 description 1
244000250129 Trigonella foenum graecum Species 0.000 description 1
101100184148 Xenopus laevis mix-a gene Proteins 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
229940040563 agaric acid Drugs 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
229910052787 antimony Inorganic materials 0.000 description 1
WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
238000010009 beating Methods 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
239000011630 iodine Substances 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
238000002955 isolation Methods 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
ZJQHPWUVQPJPQT-UHFFFAOYSA-N muscimol Chemical compound NCC1=CC(=O)NO1 ZJQHPWUVQPJPQT-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
229960001027 opium Drugs 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
239000002904 solvent Substances 0.000 description 1
210000004243 sweat Anatomy 0.000 description 1
MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
150000003503 terephthalic acid derivatives Chemical class 0.000 description 1
JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Polyamides (AREA)
Catalysts (AREA)

SU1899019A 1972-04-01 1973-03-30 Способ получени незамещенных или замещенных пара-или мета-фенилендиаминов SU495824A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19722216028 DE2216028C3 (de)	1972-04-01	1972-04-01	Verfahren zur Herstellung von unsubstituierten und substituierten p- und m-Phenylendiaminen

Publications (1)

Publication Number	Publication Date
SU495824A3 true SU495824A3 (ru)	1975-12-15

Family

ID=5840878

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU1899019A SU495824A3 (ru)	1972-04-01	1973-03-30	Способ получени незамещенных или замещенных пара-или мета-фенилендиаминов

Country Status (13)

Country	Link
JP (1)	JPS5754500B2 (it)
AT (1)	AT321887B (it)
BE (1)	BE797562A (it)
CA (1)	CA1010896A (it)
CH (1)	CH590203A5 (it)
DD (1)	DD107437A5 (it)
DE (1)	DE2216028C3 (it)
ES (1)	ES413229A1 (it)
FR (1)	FR2178975B1 (it)
GB (1)	GB1399407A (it)
IT (1)	IT988135B (it)
NL (1)	NL7304532A (it)
SU (1)	SU495824A3 (it)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4254272A (en) *	1979-02-21	1981-03-03	The Goodyear Tire & Rubber Company	Aromatic diamines and polyurethanes cured thereby
DE3126435A1 (de) *	1981-07-04	1983-01-20	Basf Ag, 6700 Ludwigshafen	Verfahren zur herstellung von gegebenenfalls zelligen polyurethan-polyharnstoff-formkoerpern und alkylsubstituierte phenylendiamine hierzu
DE3309913A1 (de) *	1983-03-19	1984-09-27	Henkel KGaA, 4000 Düsseldorf	Neue 2,4-diaminobenzolderivate als kuppler fuer oxidationshaarfaerbemittel
RU2378248C1 (ru) *	2008-10-27	2010-01-10	Открытое акционерное общество "Каустик" (ОАО "Каустик")	СПОСОБ ПОЛУЧЕНИЯ п-ФЕНИЛЕНДИАМИНА
CN102276376B (zh) *	2010-06-13	2013-08-28	华东理工大学	轴手性二胺衍生物的制备方法
EP3691785A4 (en)	2017-10-05	2021-08-04	Novomer, Inc.	ISOCYANATES, DERIVATIVES AND METHOD FOR THEIR MANUFACTURING
CN111018720B (zh) *	2019-12-16	2021-01-22	上海交通大学	间苯二胺的制备方法

1972
- 1972-04-01 DE DE19722216028 patent/DE2216028C3/de not_active Expired
1973
- 1973-03-13 IT IT4877773A patent/IT988135B/it active
- 1973-03-28 CA CA167,378A patent/CA1010896A/en not_active Expired
- 1973-03-29 DD DD16981973A patent/DD107437A5/xx unknown
- 1973-03-30 BE BE129465A patent/BE797562A/xx not_active IP Right Cessation
- 1973-03-30 GB GB1544073A patent/GB1399407A/en not_active Expired
- 1973-03-30 SU SU1899019A patent/SU495824A3/ru active
- 1973-03-30 CH CH459873A patent/CH590203A5/xx not_active IP Right Cessation
- 1973-03-30 FR FR7311668A patent/FR2178975B1/fr not_active Expired
- 1973-03-30 AT AT282373A patent/AT321887B/de not_active IP Right Cessation
- 1973-03-31 ES ES413229A patent/ES413229A1/es not_active Expired
- 1973-03-31 NL NL7304532A patent/NL7304532A/xx not_active Application Discontinuation
- 1973-04-02 JP JP3772173A patent/JPS5754500B2/ja not_active Expired

Also Published As

Publication number	Publication date
BE797562A (fr)	1973-07-16
DD107437A5 (it)	1974-08-05
DE2216028A1 (de)	1973-10-11
JPS4992031A (it)	1974-09-03
FR2178975B1 (it)	1978-03-10
JPS5754500B2 (it)	1982-11-18
NL7304532A (it)	1973-10-03
CA1010896A (en)	1977-05-24
DE2216028C3 (de)	1979-06-28
CH590203A5 (it)	1977-07-29
IT988135B (it)	1975-04-10
FR2178975A1 (it)	1973-11-16
GB1399407A (en)	1975-07-02
AT321887B (de)	1975-04-25
ES413229A1 (es)	1976-01-01
DE2216028B2 (de)	1978-11-02

Publication	Publication Date	Title
SU495824A3 (ru)	1975-12-15	Способ получени незамещенных или замещенных пара-или мета-фенилендиаминов
DK159878B (da)	1990-12-24	Fremgangsmaade til fremstilling af 2-amino-3-carbethoxyamino-6-(p-fluor-benzylamino)-pyridin-maleat
US3703542A (en)	1972-11-21	Hydroxamic acid derivatives of 1-amino-cyclohexanecarboxylic acid
DE69204806T2 (de)	1996-04-11	1-Cyanomethyl-4-carboxymethyl-3-ketopiperazine, ihre Salze und Verfahren zu ihrer Herstellung.
US2066742A (en)	1937-01-05	Antimony compounds of polyhydroxy carboxylic acids and process of making them
Cogin et al.	1951	Competition in the Binding of Long Chain Fatty Acids and Methyl Orange to Bovine Serum Albumin1
Forsman et al.	1953	The Reactions of Phenyl Esters of Phosphorous Acid with Iodine1
DE69518888T2 (de)	2001-05-10	Verfahren zur Herstellung von N-vinylverbindungen
US499927A (en)	1893-06-20	Prosper monnet
Sell et al.	1897	XCVIII.—Studies on citrazinic acid. Part V
SU857133A1 (ru)	1981-08-23	Способ получени 4-замещенных-4-карбэтокси-5-метиленпентанолидов-5
SU100591A1 (ru)	1954-11-30	Способ получени бисульфитного соединени ализарин-хинолина-3
US1485380A (en)	1924-03-04	Therapeutic compound and process of producing the same
DE2048912C3 (de)	1980-07-31	Verfahren zur Herstellung von l-Aminoalkan-l.l-diphosphonsäuren
US338365A (en)	1886-03-23	Den nachfolger
US535270A (en)	1895-03-05	Richard auschutz
US1604143A (en)	1926-10-26	Bismuth compound of aminophenols and process of making same
SU348063A1 (ru)	1976-01-15	Способ получени комплексной соли карбамида двухзамещенного фосфата меди
SU644375A3 (ru)	1979-01-25	Способ получени 3-цианамидо4-трифторметил-2,6-динитроанилинов или их основных солей
DE682256C (de)	1939-10-11	Verfahren zur Herstellung neuer saurer quartaerer Ammoniumoxalate
SU372209A1 (it)	1973-03-01
US555711A (en)	1896-03-03	Ijruno richard setfert
US708511A (en)	1902-09-09	Paramethyl-amidophenyl-glyoxylic acid and process of making same.
US913940A (en)	1909-03-02	Manufacture of homologues of para-aminophenylarsinic acids.
SU557996A1 (ru)	1977-05-15	Способ получени трехзамещенного фосфата алюмини