IL67357A - Preparation of cyclic 1,2-cis-diols from cyclic 1,2-epoxides - Google Patents

Preparation of cyclic 1,2-cis-diols from cyclic 1,2-epoxides

Info

Publication number
IL67357A
IL67357A IL67357A IL6735782A IL67357A IL 67357 A IL67357 A IL 67357A IL 67357 A IL67357 A IL 67357A IL 6735782 A IL6735782 A IL 6735782A IL 67357 A IL67357 A IL 67357A
Authority
IL
Israel
Prior art keywords
cyclic
radicals
general formula
cis
carbon atoms
Prior art date
Application number
IL67357A
Other versions
IL67357A0 (en
Original Assignee
Bayer Ag
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.)
Filing date
Publication date
Application filed by Bayer Ag filed Critical Bayer Ag
Publication of IL67357A0 publication Critical patent/IL67357A0/en
Publication of IL67357A publication Critical patent/IL67357A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/09Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
    • C07C29/095Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of esters of organic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/128Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by alcoholysis
    • C07C29/1285Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by alcoholysis of esters of organic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/09Geometrical isomers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08Systems containing only non-condensed rings with a five-membered ring the ring being saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/18Systems containing only non-condensed rings with a ring being at least seven-membered

Abstract

1. Process for the preparation of cyclic 1,2-cis-diols of the general formula I see diagramm : EP0080658,P10,F3 wherein the carbocyclic ring contains 5-7 carbon atoms and R**1 and R**2 are identical or different and independently of each other represent hydrogen or optionally substituted alkyl, cycloalkyl, alkenyl, aryl or aralkyl radicals, n represents 1, 2, 3 or 4 and R represents hydrogen, hydroxyl, halogen, cyano or optionally substituted alkyl cycloalkyl, alkenyl, aryl, aralkyl, alkoxy, alkoxycarbonyl, aryloxy, alkylthio, arylthio or heterocyclic radicals, it being possible, in the case n > 1, for the radicals R to be identical or different, and it being possible for 2 adjacent radicals R, optionally also twice, to represent a double bond, characterised in that cyclic 1,2-epoxides of the general formula II see diagramm : EP0080658,P11,F1 wherein the carbocyclic ring contains 5-7 carbon atoms and R**1 , R**2 , n and R have the abovementioned meaning, are reacted with carbon dioxide in the presence of a carbonation catalyst under pressures of 20-200 bars and at temperatures between 100 and 300 degrees C, the pressure being kept constant by pumping in further carbon dioxide until a decrease in pressure is no longer observed, - (1st stage) - and the cyclic 1,2-cis-carbonates formed in this reaction, of the general formula (III) see diagramm : EP0080658,P11,F2 wherein the carbocyclic ring again contains 5-7 carbon atoms and R**1 , R**2 , n and R have the abovementioned meaning, are hydrolysed with water, aqueous salt solutions, dilute aqueous acids or bases or solvolysed with a solution of an alcoholate in an alcohol, in each case at an elevated temperature, and if appropriate, under an elevated pressure (2nd stage).
IL67357A 1981-12-02 1982-11-29 Preparation of cyclic 1,2-cis-diols from cyclic 1,2-epoxides IL67357A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19813147737 DE3147737A1 (en) 1981-12-02 1981-12-02 METHOD FOR PRODUCING CYCLIC 1,2-CIS-DIOLS FROM CYCLIC 1,2-EPOXIES

Publications (2)

Publication Number Publication Date
IL67357A0 IL67357A0 (en) 1983-03-31
IL67357A true IL67357A (en) 1986-02-28

Family

ID=6147730

Family Applications (1)

Application Number Title Priority Date Filing Date
IL67357A IL67357A (en) 1981-12-02 1982-11-29 Preparation of cyclic 1,2-cis-diols from cyclic 1,2-epoxides

Country Status (4)

Country Link
EP (1) EP0080658B1 (en)
JP (1) JPS58103330A (en)
DE (2) DE3147737A1 (en)
IL (1) IL67357A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2636940C1 (en) * 2017-03-30 2017-11-29 Федеральное государственное бюджетное образовательное учреждение высшего образования "Ярославский государственный технический университет" ФГБОУВО "ЯГТУ" Method of producing cyclopentencharbonate by catalytic carboxylation of 1,2-epoxycyclopentane

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2773070A (en) * 1952-10-31 1956-12-04 Jefferson Chem Co Inc Catalytic process for producing alkylene carbonates
DE1096348B (en) * 1959-10-26 1961-01-05 Fmc Corp Process for the production of sobrerol by treating ª ‡ -pinene oxide
DE1169459B (en) * 1960-06-09 1964-05-06 Basf Ag Process for the production of alkylene carbonates
DE1793247C3 (en) * 1968-08-21 1973-11-29 Wsesojusnij Nautschno-Issledowatel' Skij Institut Neftechimitscheskich Prozessow, Leningrad (Sowjetunion) Process for the production of alkylene glycols
DE2740243A1 (en) * 1977-09-07 1979-03-15 Bayer Ag PROCESS FOR THE PRODUCTION OF DIALKYLCARBONATES
US4187373A (en) * 1978-10-02 1980-02-05 American Cyanamid Company Novel dihydrobenzanthracene derivatives
CA1107301A (en) * 1977-12-22 1981-08-18 Union Carbide Corporation Hydrolysis of alkylene carbonates to alkylene glycols
US4314945A (en) * 1977-12-22 1982-02-09 Union Carbide Corporation Alkylene carbonate process
CA1133522A (en) * 1978-06-20 1982-10-12 Glenn A. Taylor Process for hydrolyzing alkylene oxides to alkylene glycols

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2636940C1 (en) * 2017-03-30 2017-11-29 Федеральное государственное бюджетное образовательное учреждение высшего образования "Ярославский государственный технический университет" ФГБОУВО "ЯГТУ" Method of producing cyclopentencharbonate by catalytic carboxylation of 1,2-epoxycyclopentane

Also Published As

Publication number Publication date
EP0080658A1 (en) 1983-06-08
EP0080658B1 (en) 1987-09-30
IL67357A0 (en) 1983-03-31
JPS58103330A (en) 1983-06-20
DE3147737A1 (en) 1983-06-09
DE3277409D1 (en) 1987-11-05

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