CA1070289A - Melanges d'acides monocarboxyliques a ramifications multiples et methode pour leur preparation - Google Patents

Melanges d'acides monocarboxyliques a ramifications multiples et methode pour leur preparation

Info

Publication number: CA1070289A
Authority: CA; Canada
Prior art keywords: methyl; ethyl; butyl; weight; acids
Prior art date: 1975-05-19
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

CA252,178A

Other languages

English (en)

Inventor

Rakhil K. Freidlina

Alexandr B. Terentiev

Dmitry I. Povolotsky

Vladimir M. Mikhailov

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.)

INSTITUT ELEMENTOORGANICHESKIKH SOEDINENY AKADEMII NAUK SSSR

Original Assignee

INSTITUT ELEMENTOORGANICHESKIKH SOEDINENY AKADEMII NAUK SSSR

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.)

1975-05-19

Filing date

1976-05-11

Publication date

1980-01-22

1975-05-19 Priority claimed from SU752130253A external-priority patent/SU615059A1/ru

1976-05-11 Application filed by INSTITUT ELEMENTOORGANICHESKIKH SOEDINENY AKADEMII NAUK SSSR filed Critical INSTITUT ELEMENTOORGANICHESKIKH SOEDINENY AKADEMII NAUK SSSR

1980-01-22 Application granted granted Critical

1980-01-22 Publication of CA1070289A publication Critical patent/CA1070289A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 39
150000002763 monocarboxylic acids Chemical class 0.000 title claims abstract description 12
238000004519 manufacturing process Methods 0.000 title claims abstract description 7
239000002253 acid Substances 0.000 claims abstract description 45
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 22
238000000034 method Methods 0.000 claims abstract description 21
230000008569 process Effects 0.000 claims abstract description 21
150000007513 acids Chemical class 0.000 claims abstract description 18
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 13
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 11
150000002978 peroxides Chemical class 0.000 claims abstract description 10
150000001735 carboxylic acids Chemical class 0.000 claims abstract description 8
239000011541 reaction mixture Substances 0.000 claims abstract description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 4
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 4
238000000926 separation method Methods 0.000 claims abstract description 4
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 3
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
239000001257 hydrogen Substances 0.000 claims abstract description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract 8
239000004711 α-olefin Substances 0.000 claims abstract 5
239000003999 initiator Substances 0.000 claims description 12
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 6
BLCKNMAZFRMCJJ-UHFFFAOYSA-N cyclohexyl cyclohexyloxycarbonyloxy carbonate Chemical compound C1CCCCC1OC(=O)OOC(=O)OC1CCCCC1 BLCKNMAZFRMCJJ-UHFFFAOYSA-N 0.000 claims description 4
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 claims description 4
-1 butyl,hexyl Chemical group 0.000 claims description 2
230000003993 interaction Effects 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 abstract description 3
238000000605 extraction Methods 0.000 abstract description 3
238000002360 preparation method Methods 0.000 abstract description 3
238000009854 hydrometallurgy Methods 0.000 abstract 1
239000003973 paint Substances 0.000 abstract 1
239000000047 product Substances 0.000 abstract 1
239000002699 waste material Substances 0.000 abstract 1
239000002351 wastewater Substances 0.000 abstract 1
239000000243 solution Substances 0.000 description 9
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 8
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 7
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
125000001424 substituent group Chemical group 0.000 description 7
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 6
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
238000010438 heat treatment Methods 0.000 description 6
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 6
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 5
230000002378 acidificating effect Effects 0.000 description 5
150000001336 alkenes Chemical class 0.000 description 5
238000009835 boiling Methods 0.000 description 5
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 4
229910052742 iron Inorganic materials 0.000 description 4
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 4
101100087530 Caenorhabditis elegans rom-1 gene Proteins 0.000 description 3
101100305983 Mus musculus Rom1 gene Proteins 0.000 description 3
240000001987 Pyrus communis Species 0.000 description 3
229910000831 Steel Inorganic materials 0.000 description 3
150000002500 ions Chemical class 0.000 description 3
235000019260 propionic acid Nutrition 0.000 description 3
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
239000010959 steel Substances 0.000 description 3
229940005605 valeric acid Drugs 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 2
239000004411 aluminium Substances 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
238000005194 fractionation Methods 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
230000008707 rearrangement Effects 0.000 description 2
241000894007 species Species 0.000 description 2
239000002966 varnish Substances 0.000 description 2
PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical compound CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 description 1
HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
102100025597 Caspase-4 Human genes 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
241000405147 Hermes Species 0.000 description 1
101100273284 Homo sapiens CASP4 gene Proteins 0.000 description 1
241001163743 Perlodes Species 0.000 description 1
101150057388 Reln gene Proteins 0.000 description 1
208000027697 autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency Diseases 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
IYRDVAUFQZOLSB-UHFFFAOYSA-N copper iron Chemical compound [Fe].[Cu] IYRDVAUFQZOLSB-UHFFFAOYSA-N 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000003756 stirring Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/126—Acids containing more than four carbon atoms
- C07C53/128—Acids containing more than four carbon atoms the carboxylic group being bound to a carbon atom bound to at least two other carbon atoms, e.g. neo-acids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/353—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by isomerisation; by change of size of the carbon skeleton

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Manufacture And Refinement Of Metals (AREA)

CA252,178A 1975-05-19 1976-05-11 Melanges d'acides monocarboxyliques a ramifications multiples et methode pour leur preparation Expired CA1070289A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
SU752130253A SU615059A1 (ru)	1975-05-19	1975-05-19	Смесь полиразветвленных монокарбоновых кислот в качестве солеобразующего агента и способ ее получени
JP5772476A JPS52142008A (en)	1975-05-19	1976-05-19	Mixtures of poly branch monocarboxylic acid

Publications (1)

Publication Number	Publication Date
CA1070289A true CA1070289A (fr)	1980-01-22

Family

ID=26398787

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA252,178A Expired CA1070289A (fr)	1975-05-19	1976-05-11	Melanges d'acides monocarboxyliques a ramifications multiples et methode pour leur preparation

Country Status (9)

Country	Link
JP (1)	JPS52142008A (fr)
AT (1)	AT347420B (fr)
CA (1)	CA1070289A (fr)
CH (1)	CH629174A5 (fr)
DE (1)	DE2621526C3 (fr)
DK (1)	DK218676A (fr)
GB (1)	GB1553702A (fr)
NL (1)	NL7605350A (fr)
SE (1)	SE411895B (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1339034C (fr) *	1988-08-22	1997-04-01	Paul A. Tremblay	Complexes de platine d'isomeres uniques d'acides neoalkyliques
ZA933123B (en) *	1992-05-06	1993-11-30	Shell Res Ltd	Saturated, monocarboxylic acids, the preparation thereof, and derivatives therefrom
CN1283219A (zh)	1997-10-23	2001-02-07	宝洁公司	脂肪酸、皂、表面活性剂体系及以其为基础的消费品
WO2000007971A1 (fr) *	1998-08-06	2000-02-17	Exxon Chemical Patents Inc.	Acides neocarboxyliques et procede pour leur preparation
US6890894B2 (en)	2000-02-22	2005-05-10	The Procter & Gamble Company	Fatty acids, soaps surfactant systems, and consumer products based thereon

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5623973B2 (fr) *	1972-02-12	1981-06-03

1976
- 1976-05-11 CA CA252,178A patent/CA1070289A/fr not_active Expired
- 1976-05-12 CH CH595876A patent/CH629174A5/de not_active IP Right Cessation
- 1976-05-14 DE DE2621526A patent/DE2621526C3/de not_active Expired
- 1976-05-18 SE SE7605626A patent/SE411895B/xx not_active IP Right Cessation
- 1976-05-18 DK DK218676A patent/DK218676A/da not_active Application Discontinuation
- 1976-05-19 AT AT364676A patent/AT347420B/de not_active IP Right Cessation
- 1976-05-19 NL NL7605350A patent/NL7605350A/xx unknown
- 1976-05-19 GB GB20754/76A patent/GB1553702A/en not_active Expired
- 1976-05-19 JP JP5772476A patent/JPS52142008A/ja active Pending

Also Published As

Publication number	Publication date
NL7605350A (nl)	1976-11-23
JPS52142008A (en)	1977-11-26
CH629174A5 (en)	1982-04-15
DE2621526A1 (de)	1976-12-30
SE7605626L (sv)	1976-11-20
AT347420B (de)	1978-12-27
ATA364676A (de)	1978-05-15
DK218676A (da)	1976-11-20
GB1553702A (en)	1979-09-26
SE411895B (sv)	1980-02-11
DE2621526B2 (de)	1980-06-26
DE2621526C3 (de)	1981-02-26

Legal Events

Date	Code	Title	Description
1997-01-22	MKEX	Expiry

Publication	Publication Date	Title
Rauhut et al.	1961	The free radical addition of phosphines to unsaturated compounds
CA1070289A (fr)	1980-01-22	Melanges d'acides monocarboxyliques a ramifications multiples et methode pour leur preparation
AU714151B2 (en)	1999-12-23	Processes for the preparation of 3-(methylthio)propanal and 2-hydroxy-4-(methylthio)butanenitrile
CA1092612A (fr)	1980-12-30	Procede d'obtention de 2,4,6-tri-(butyl-4- hydroxybenzyle 3,5-ditertiaire) mesitylene
Mariella	1947	Condensations of unsymmetrical ketones. I. condensations with ethyl formate
US3948803A (en)	1976-04-06	Catalyst
JPS61271281A (ja)	1986-12-01	Ｓ−トリアジン誘導体の製法
JPH05310640A (ja)	1993-11-22	ヒドロキシフェニルカルボキシレートの製造方法
US4135047A (en)	1979-01-16	Preparation of thioethers using a benzopinacol initiator
US5087757A (en)	1992-02-11	Preparation of alkylthioethylamine salts
US4517122A (en)	1985-05-14	Cyclic peptides
Wildschut et al.	1969	Alkylthiolation of ambident anions derived from some unsaturated organic sulfides
CN114181118A (zh)	2022-03-15	一种脂肪酰基牛磺酸盐的合成工艺
Hauser et al.	1959	Formation and Certain Condensations of the Dicarbanions of Dibenzyl Ketone and Dibenzyl Sulfone by Means of Potassium Amide in Liquid Ammonia1, 2
JPH0383954A (ja)	1991-04-09	第三アミン中の第一および第二アミンの含量を減少させる方法
CA1076136A (fr)	1980-04-22	Preparation de l'acide 5-oxohexanoique et de ses derives
DE2450617A1 (de)	1975-04-30	Thiazolderivate, ihre salze, verfahren zu ihrer herstellung und arzneimittel
SU798102A1 (ru)	1981-01-23	Способ совместного получени , , -ТРибЕНзилгЕКСАгидРО-ТРиАзиНА-1,3,5 и -МЕТилбЕНзил-АМиНО- -бЕНзилиМиНОМЕТилЕНА
US3082235A (en)	1963-03-19	1-oxa-2-alumina-3-thio cyclo ketones and their preparation
JPS61500548A (ja)	1986-03-27	β−（４−ヒドロキシ−３，５−ジ−第三級ブチルフェニル）プロピオン酸アルキルエステルの製法
CA2019769C (fr)	1999-01-26	Acides 3-(alkylthio)propioniques et leurs derives
US2531283A (en)	1950-11-21	Preparation of thioacetamide
JPH0649667B2 (ja)	1994-06-29	２，２−ビス（４′−アクリロイルオキシ−３′，５′−ジブロモフエニル）プロパンの製造法
CN112239417A (zh)	2021-01-19	一种2-羟乙基脲的制备方法
US3417121A (en)	1968-12-17	Substituted 1,2-silthiacyclopentanes and process for producing the same