SU413673A3 - Способ получения диамида бяс-щавелевойкислоты12 - Google Patents

Способ получения диамида бяс-щавелевойкислоты12

Info

Publication number: SU413673A3
Authority: SU; USSR - Soviet Union
Prior art keywords: formula; diagnobas; obtaining; compound; diamide
Prior art date: 1970-04-29

Application number

SU1653203A

Other languages

English (en)

Russian (ru)

Original Assignee

Иностранцы Макс Динненбергер , Ханс Рудольф Биланд

Иностранна Циба Гейги

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.)

1970-04-29

Filing date

1971-04-28

Publication date

1974-01-30

1971-04-28 Application filed by Иностранцы Макс Динненбергер , Ханс Рудольф Биланд, Иностранна Циба Гейги filed Critical Иностранцы Макс Динненбергер , Ханс Рудольф Биланд

1974-01-30 Application granted granted Critical

1974-01-30 Publication of SU413673A3 publication Critical patent/SU413673A3/ru

Links

238000000034 method Methods 0.000 title description 7
150000001875 compounds Chemical class 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
230000003078 antioxidant effect Effects 0.000 description 3
YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical class NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000000463 material Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
230000003064 anti-oxidating effect Effects 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000013078 crystal Substances 0.000 description 1
150000001470 diamides Chemical class 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
-1 halide ester Chemical class 0.000 description 1
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
XHTYLMIRTKBVHT-UHFFFAOYSA-N oxamide Chemical compound NC(=O)C(N)=O.NC(=O)C(N)=O XHTYLMIRTKBVHT-UHFFFAOYSA-N 0.000 description 1
229960003742 phenol Drugs 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/20—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing nitrogen and oxygen
- C09K15/22—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing nitrogen and oxygen containing an amide or imide moiety
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/20—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing nitrogen and oxygen
- C09K15/24—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing nitrogen and oxygen containing a phenol or quinone moiety
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B5/00—Preserving by using additives, e.g. anti-oxidants
- C11B5/0042—Preserving by using additives, e.g. anti-oxidants containing nitrogen
- C11B5/0057—Amides or imides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Materials Engineering (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Compositions Of Macromolecular Compounds (AREA)
Anti-Oxidant Or Stabilizer Compositions (AREA)

SU1653203A 1970-04-29 1971-04-28 Способ получения диамида бяс-щавелевойкислоты12 SU413673A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH646570A CH534539A (de)	1970-04-29	1970-04-29	Verwendung von Bis-oxalsäurediamiden als Antioxydantien für organische Materialien

Publications (1)

Publication Number	Publication Date
SU413673A3 true SU413673A3 (ru)	1974-01-30

Family

ID=4310055

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU1653203A SU413673A3 (ru)	1970-04-29	1971-04-28	Способ получения диамида бяс-щавелевойкислоты12

Country Status (8)

Country	Link
AT (1)	AT309826B (de)
CA (1)	CA924327A (de)
CH (1)	CH534539A (de)
DE (1)	DE2120954A1 (de)
FR (1)	FR2090870A5 (de)
GB (1)	GB1325944A (de)
NL (1)	NL7105824A (de)
SU (1)	SU413673A3 (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4104287A (en) *	1973-02-24	1978-08-01	Basf Aktiengesellschaft	4-M,M'-Di-t-butyl-p-hydroxyphenyl) butyl-2 compounds
EP0002616B1 (de) *	1977-12-21	1983-03-30	Uniroyal, Inc.	Oxalsäureamidderivate, deren Verwendung als Stabilisierungsmittel für organische Materialien und stabilisierte Materialien, die diese Oxalsäureamidderivate enthalten
EP2736971A1 (de)	2011-07-29	2014-06-04	Dow Global Technologies LLC	Semikristalline polyolefinzusammensetzung, verfahren zu ihrer herstellung und daraus hergestellte artikel

1970
- 1970-04-29 CH CH646570A patent/CH534539A/de not_active IP Right Cessation
1971
- 1971-04-23 AT AT352471A patent/AT309826B/de not_active IP Right Cessation
- 1971-04-28 FR FR7115172A patent/FR2090870A5/fr not_active Expired
- 1971-04-28 GB GB1190871A patent/GB1325944A/en not_active Expired
- 1971-04-28 NL NL7105824A patent/NL7105824A/xx unknown
- 1971-04-28 DE DE19712120954 patent/DE2120954A1/de active Pending
- 1971-04-28 CA CA111574A patent/CA924327A/en not_active Expired
- 1971-04-28 SU SU1653203A patent/SU413673A3/ru active

Also Published As

Publication number	Publication date
CA924327A (en)	1973-04-10
GB1325944A (en)	1973-08-08
CH534539A (de)	1973-03-15
AT309826B (de)	1973-09-10
FR2090870A5 (de)	1972-01-14
DE2120954A1 (de)	1971-11-18
NL7105824A (de)	1971-11-02

Publication	Publication Date	Title
Yale	1971	Formylation of amines with phenyl formate
SU470112A3 (ru)	1975-05-05	Способ получени производных 4-пиперидинола
US3652671A (en)	1972-03-28	Process for making a cationic methacrylamide
US4716244A (en)	1987-12-29	Process for the preparation of sterically hindered hydroxyphenylcarboxylic acid esters
DE3209800C2 (de)	1990-03-08	Verfahren zur Herstellung von N-(tert. Aminoalkyl)acrylamiden
US2453103A (en)	1948-11-02	Decarboxylation of 3,4-dihydroxy-2,5-dicarboxythiophene
US3860598A (en)	1975-01-14	Process for the production of benzylidene compounds
SU413673A3 (ru)	1974-01-30	Способ получения диамида бяс-щавелевойкислоты12
US4517122A (en)	1985-05-14	Cyclic peptides
US4285872A (en)	1981-08-25	Method for producing glycidyl (metha)acrylate
US3119823A (en)	1964-01-28	Process for preparation of o-hydroxyphenyl-triazines
US3636036A (en)	1972-01-18	Alkyl substituted phenylene diisonitriles
SU628811A3 (ru)	1978-10-15	Способ получени производных дифениламина
SU422138A3 (de)	1974-03-30
Durrell et al.	1963	Fluorocarbon Nitrogen Compounds. IX. The Reaction of Nitriles with Carboxylic Acids1
US3066167A (en)	1962-11-27	4-amino-3, 5-dichloro-benzamides
US3743668A (en)	1973-07-03	Cyanoethylation of aminophenols
Galat	1948	A Synthesis of α, β-Unsaturated Amides
US2848478A (en)	1958-08-19	3-hydrocarbo-2-cyclobutene-1, 2-dicarboxylic acids and their preparation
RU2067575C1 (ru)	1996-10-10	4-ацетил-5-п-иодфенил-1-карбоксиметил-3-гидрокси-2,5-дигидропиррол-2-он, проявляющий анальгетическую активность
US4600535A (en)	1986-07-15	Cyclic peptides
US3746757A (en)	1973-07-17	Process for manufacturing 6-nitro-2-oximinohexanoic acid derivatives
US3109022A (en)	1963-10-29	Nu-aryl anthranilic acids
US3103520A (en)	1963-09-10	Aminobenzoxacycloalkanes
US3511873A (en)	1970-05-12	N-(4-carboxyphenyl)anthranilic acid