CA1029045A - Extraction process of cycloaliphatic hydroperoxides - Google Patents

Extraction process of cycloaliphatic hydroperoxides

Info

Publication number: CA1029045A
Authority: CA; Canada
Prior art keywords: par; que; hydroperoxyde; procédé; caractérisé
Prior art date: 1973-06-04
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

CA201,142A

Other languages

English (en)

French (fr)

Other versions

CA201142S (en

Inventor

Lucien Billet

Michel Jouffret

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.)

Rhone Poulenc SA

Original Assignee

Rhone Poulenc SA

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.)

1973-06-04

Filing date

1974-05-29

Publication date

1978-04-04

1974-05-29 Application filed by Rhone Poulenc SA filed Critical Rhone Poulenc SA

1978-04-04 Application granted granted Critical

1978-04-04 Publication of CA1029045A publication Critical patent/CA1029045A/en

Status Expired legal-status Critical Current

Links

238000000605 extraction Methods 0.000 title claims abstract description 21
150000002432 hydroperoxides Chemical class 0.000 title abstract 2
238000007254 oxidation reaction Methods 0.000 claims abstract description 10
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 5
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims description 5
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 3
150000004649 carbonic acid derivatives Chemical class 0.000 claims description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 2
101150093826 par1 gene Proteins 0.000 claims 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 6
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract description 3
238000000034 method Methods 0.000 abstract description 3
PPQREHKVAOVYBT-UHFFFAOYSA-H dialuminum;tricarbonate Chemical compound [Al+3].[Al+3].[O-]C([O-])=O.[O-]C([O-])=O.[O-]C([O-])=O PPQREHKVAOVYBT-UHFFFAOYSA-H 0.000 abstract 2
229940118662 aluminum carbonate Drugs 0.000 abstract 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
125000004432 carbon atom Chemical group C* 0.000 abstract 1
229930195733 hydrocarbon Natural products 0.000 abstract 1
150000002430 hydrocarbons Chemical class 0.000 abstract 1
230000003647 oxidation Effects 0.000 abstract 1
229910052760 oxygen Inorganic materials 0.000 abstract 1
239000001301 oxygen Substances 0.000 abstract 1
239000002904 solvent Substances 0.000 abstract 1
-1 pentaméthylene Chemical group 0.000 description 8
150000003254 radicals Chemical class 0.000 description 6
BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 3
229940082150 encore Drugs 0.000 description 3
239000000203 mixture Substances 0.000 description 3
238000006677 Appel reaction Methods 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 1
UDKCHVLMFQVBAA-UHFFFAOYSA-M Choline salicylate Chemical compound C[N+](C)(C)CCO.OC1=CC=CC=C1C([O-])=O UDKCHVLMFQVBAA-UHFFFAOYSA-M 0.000 description 1
101100421144 Danio rerio selenoo1 gene Proteins 0.000 description 1
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
101100490479 Lactococcus lactis subsp. lactis (strain IL1403) addA gene Proteins 0.000 description 1
101100000975 Lactococcus lactis subsp. lactis (strain IL1403) rexB gene Proteins 0.000 description 1
101100202896 Mus musculus Selenoo gene Proteins 0.000 description 1
240000001987 Pyrus communis Species 0.000 description 1
208000037656 Respiratory Sounds Diseases 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
241001080024 Telles Species 0.000 description 1
230000009471 action Effects 0.000 description 1
238000013019 agitation Methods 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000010504 bond cleavage reaction Methods 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
230000004927 fusion Effects 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
101150006061 neur gene Proteins 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
206010037833 rales Diseases 0.000 description 1
230000007017 scission Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
- C07C407/003—Separation; Purification; Stabilisation; Use of additives
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Extraction Or Liquid Replacement (AREA)

CA201,142A 1973-06-04 1974-05-29 Extraction process of cycloaliphatic hydroperoxides Expired CA1029045A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR7320225A FR2231661B1 (de)	1973-06-04	1973-06-04

Publications (1)

Publication Number	Publication Date
CA1029045A true CA1029045A (en)	1978-04-04

Family

ID=9120460

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA201,142A Expired CA1029045A (en)	1973-06-04	1974-05-29	Extraction process of cycloaliphatic hydroperoxides

Country Status (14)

Country	Link
US (1)	US3956397A (de)
JP (1)	JPS5019737A (de)
AT (1)	AT331208B (de)
BE (1)	BE815901A (de)
BR (1)	BR7404437D0 (de)
CA (1)	CA1029045A (de)
DD (1)	DD111900A5 (de)
DE (1)	DE2426864A1 (de)
FR (1)	FR2231661B1 (de)
GB (1)	GB1450754A (de)
IT (1)	IT1014770B (de)
LU (1)	LU70207A1 (de)
NL (1)	NL7407081A (de)
SU (1)	SU583747A3 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2955322B1 (fr) *	2010-01-21	2013-09-06	Rhodia Operations	Procede de fabrication d'un hydroperoxyde d'alkyle

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2430865A (en) *	1944-02-17	1947-11-18	Union Oil Co	Naphthene peroxides
US3256341A (en) *	1960-12-02	1966-06-14	Union Carbide Corp	Extraction of 1, 2, 3, 4-tetrahydronaphthalene hydroperoxide
FR1347591A (fr) *	1963-02-19	1963-12-27	British Petroleum Co	Procédé de séparation mutuelle d'hydroperoxydes organiques et d'hydrocarbures éthyléniques à partir de mélagnes qui les contiennent
FR1491518A (fr) *	1966-06-30	1967-08-11	Rhone Poulenc Sa	Préparation d'hydroperoxydes

1973
- 1973-06-04 FR FR7320225A patent/FR2231661B1/fr not_active Expired
1974
- 1974-05-27 NL NL7407081A patent/NL7407081A/xx not_active Application Discontinuation
- 1974-05-29 CA CA201,142A patent/CA1029045A/en not_active Expired
- 1974-05-30 BR BR4437/74A patent/BR7404437D0/pt unknown
- 1974-05-31 JP JP49061758A patent/JPS5019737A/ja active Pending
- 1974-05-31 US US05/475,042 patent/US3956397A/en not_active Expired - Lifetime
- 1974-05-31 DD DD178908A patent/DD111900A5/xx unknown
- 1974-05-31 LU LU70207A patent/LU70207A1/xx unknown
- 1974-06-03 SU SU7402030716A patent/SU583747A3/ru active
- 1974-06-03 GB GB2447874A patent/GB1450754A/en not_active Expired
- 1974-06-04 IT IT23602/74A patent/IT1014770B/it active
- 1974-06-04 AT AT458374A patent/AT331208B/de not_active IP Right Cessation
- 1974-06-04 BE BE145065A patent/BE815901A/xx unknown
- 1974-06-04 DE DE19742426864 patent/DE2426864A1/de not_active Withdrawn

Also Published As

Publication number	Publication date
JPS5019737A (de)	1975-03-01
DD111900A5 (de)	1975-03-12
GB1450754A (en)	1976-09-29
FR2231661A1 (de)	1974-12-27
IT1014770B (it)	1977-04-30
BE815901A (fr)	1974-12-04
BR7404437D0 (pt)	1975-09-02
FR2231661B1 (de)	1976-05-07
LU70207A1 (de)	1975-02-24
SU583747A3 (ru)	1977-12-05
NL7407081A (de)	1974-12-06
ATA458374A (de)	1975-11-15
US3956397A (en)	1976-05-11
DE2426864A1 (de)	1975-01-02
AT331208B (de)	1976-08-10

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