GB1374644A

GB1374644A – Process for producing alpha,beta-unsaturated ketones and alcohols from bicyclic dompounds
– Google Patents

GB1374644A – Process for producing alpha,beta-unsaturated ketones and alcohols from bicyclic dompounds
– Google Patents
Process for producing alpha,beta-unsaturated ketones and alcohols from bicyclic dompounds

Info

Publication number
GB1374644A

GB1374644A
GB2834272A
GB2834272A
GB1374644A
GB 1374644 A
GB1374644 A
GB 1374644A
GB 2834272 A
GB2834272 A
GB 2834272A
GB 2834272 A
GB2834272 A
GB 2834272A
GB 1374644 A
GB1374644 A
GB 1374644A
Authority
GB
United Kingdom
Prior art keywords
chr
alcohols
unsaturated ketones
bicyclic
dompounds
Prior art date
1971-06-21
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
GB2834272A
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.)

International Flavors and Fragrances Inc

Original Assignee
International Flavors and Fragrances Inc
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.)
1971-06-21
Filing date
1972-06-16
Publication date
1974-11-20

1972-06-16
Application filed by International Flavors and Fragrances Inc
filed
Critical
International Flavors and Fragrances Inc

1974-11-20
Publication of GB1374644A
publication
Critical
patent/GB1374644A/en

Status
Expired
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

Classifications

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS

C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring

C07C29/48—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups

C07C29/50—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups with molecular oxygen only

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

C07C45/34—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 in unsaturated compounds

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

C11B9/00—Essential oils; Perfumes

C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings

C11B9/0046—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings

C11B9/0049—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms

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

C11B9/00—Essential oils; Perfumes

C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings

C11B9/0046—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings

C11B9/0049—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms

C11B9/0053—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms both rings being six-membered

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS

C07C2602/00—Systems containing two condensed rings

C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common

C07C2602/14—All rings being cycloaliphatic

C07C2602/24—All rings being cycloaliphatic the ring system containing nine carbon atoms, e.g. perhydroindane

Abstract

1374644 α,#-Unsaturated ketones and alcohols from bicyclic compounds INTERNATIONAL FLAVORS & FRAGRANCES Inc 16 June 1972 [21 June 1971] 28342/72 Heading C2C Bicyclic compounds of formula where R 1 , R 2 , R 3 and R 4 are C 1 -C 6 alkyl, X is -CHR 5 – or -CHR 5 -CHR 6 -, Y is -CHR 7 or -CHR 7 -CHR 8 -, and R 5, R 6 , R 7 and R 8 are hydrogen or C 1 to C 6 alkyl, are oxidized with oxygen (either pure, as air, or admixed with inert gases such as nitrogen, argon or helium), in the presence of up to 20% by wt. of a metal organic salt catalyst containing a metal having an atomic number of from 24 to 30 to give α,#-unsaturated ketones and alcohols of formulae These compounds are used as perfume compositions.

GB2834272A
1971-06-21
1972-06-16
Process for producing alpha,beta-unsaturated ketones and alcohols from bicyclic dompounds

Expired

GB1374644A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

US00155327A

US3847993A
(en)

1971-06-21
1971-06-21
Allylic oxidation of bicyclic hydrocarbons to alcohols and ketones

Publications (1)

Publication Number
Publication Date

GB1374644A
true

GB1374644A
(en)

1974-11-20

Family
ID=22554992
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

GB2834272A
Expired

GB1374644A
(en)

1971-06-21
1972-06-16
Process for producing alpha,beta-unsaturated ketones and alcohols from bicyclic dompounds

Country Status (13)

Country
Link

US
(1)

US3847993A
(en)

JP
(1)

JPS5125018B1
(en)

AU
(1)

AU456868B2
(en)

BE
(1)

BE785208A
(en)

BR
(1)

BR7203385D0
(en)

CA
(1)

CA954533A
(en)

CH
(1)

CH541525A
(en)

DE
(1)

DE2220820C3
(en)

FR
(1)

FR2143142B1
(en)

GB
(1)

GB1374644A
(en)

IT
(1)

IT958080B
(en)

NL
(1)

NL7204806A
(en)

SU
(1)

SU501666A3
(en)

Families Citing this family (18)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US4393244A
(en)

*

1981-08-26
1983-07-12
Indian Explosives Limited
Method and the manufacture of cyclic mono and/or diketones from cyclic mono or sesqui terpenes by catalytic oxidation

US4617146A
(en)

*

1983-01-13
1986-10-14
Givaudan Corporation
Substituted bicyclo[4.3.0]non-1(6)-en-8-yl methyl ketones and fragrance and flavor compositions

US4520032A
(en)

*

1984-03-14
1985-05-28
International Flavors & Fragrances Inc.
Use in augmenting or enhancing the aroma or taste of foodstuffs or chewing gums of tetrahydro-1,1,2,3,3-pentamethyl-3A[4H]-indanol

US4548821A
(en)

*

1984-03-14
1985-10-22
International Flavors & Fragrances Inc.
Flavoring with tertiary pentamethylindanol derivatives

US4535192A
(en)

*

1984-03-14
1985-08-13
International Flavors & Fragrances Inc.
Tertiary pentamethylindanol derivatives and organoleptic uses thereof

US4572796A
(en)

*

1984-05-24
1986-02-25
International Flavors & Fragrances Inc.
1,1,4,7-Tetramethyl-3-indanone, product produced thereby and organoleptic uses thereof

US4532357A
(en)

*

1984-05-24
1985-07-30
International Flavors & Fragrances Inc.
Process for producing 1,1-dimethyl-3-indanones, products produced thereby and organoleptic uses thereof

DE3835190A1
(en)

*

1988-10-15
1990-04-26
Henkel Kgaa

ISOMERE TRIMETHYLBICYCLO (4.3.0) NONAN DERIVATIVES

US5164365A
(en)

*

1990-03-02
1992-11-17
Givaudan Corporation
1,1,2,3,3,6-hexamethyl-4,5,6,7-tetrahydro-5-indanone and fragrance compositions containing same

US5137869A
(en)

*

1991-09-13
1992-08-11
International Flavors & Fragrances Inc.
Methyl substituted tetrahydroindanone and perfumery uses thereof

ES2192010T3
(en)

*

1998-10-26
2003-09-16
Firmenich & Cie

NEW BICYCLE KETONS AND ITS USE IN THE AREA OF PERFUMERIA.

US6632788B2
(en)

2001-05-17
2003-10-14
International Flavors & Fragrances Inc.
Polyalkylbicylic derivatives

US7312187B2
(en)

*

2001-05-17
2007-12-25
International Flavors & Fragrances Inc.
Polyalkylbicyclic derivatives

US7115553B2
(en)

*

2003-07-10
2006-10-03
International Flavors & Fragrances Inc.
Acetonide fragrance compound

RU2006122944A
(en)

*

2003-11-28
2008-01-10
Фирмениш Са (Ch)

MUSCULAR AROMATIC COMPOSITION

ES2745956T3
(en)

2009-09-23
2020-03-04
Int Flavors & Fragrances Inc

Allyl oxidation method for fragrance preparation using organometallic compounds and gold catalysts

EP3257831B1
(en)

2016-06-16
2019-11-27
International Flavors & Fragrances Inc.
Circular economy methods of preparing unsaturated compounds

CN112694597B
(en)

*

2020-12-24
2022-07-01
山东天茂新材料科技股份有限公司
Preparation method of high-modulus heterocyclic epoxy resin

1971

1971-06-21
US
US00155327A
patent/US3847993A/en
not_active
Expired – Lifetime

1972

1972-04-10
CA
CA139,339A
patent/CA954533A/en
not_active
Expired

1972-04-11
NL
NL7204806A
patent/NL7204806A/xx
unknown

1972-04-14
AU
AU41187/72A
patent/AU456868B2/en
not_active
Expired

1972-04-27
DE
DE2220820A
patent/DE2220820C3/en
not_active
Expired

1972-05-26
BR
BR3385/72A
patent/BR7203385D0/en
unknown

1972-05-26
IT
IT50514/72A
patent/IT958080B/en
active

1972-06-14
SU
SU1797763A
patent/SU501666A3/en
active

1972-06-16
JP
JP47059655A
patent/JPS5125018B1/ja
active
Pending

1972-06-16
CH
CH909572A
patent/CH541525A/en
not_active
IP Right Cessation

1972-06-16
GB
GB2834272A
patent/GB1374644A/en
not_active
Expired

1972-06-20
FR
FR7222241A
patent/FR2143142B1/fr
not_active
Expired

1972-06-21
BE
BE785208A
patent/BE785208A/en
unknown

Also Published As

Publication number
Publication date

CH541525A
(en)

1973-09-15

DE2220820A1
(en)

1973-01-11

US3847993A
(en)

1974-11-12

IT958080B
(en)

1973-10-20

AU456868B2
(en)

1974-12-13

BE785208A
(en)

1972-12-21

SU501666A3
(en)

1976-01-30

AU4118772A
(en)

1973-10-18

CA954533A
(en)

1974-09-10

DE2220820B2
(en)

1975-04-30

FR2143142B1
(en)

1977-12-23

BR7203385D0
(en)

1973-05-31

DE2220820C3
(en)

1976-01-02

JPS5125018B1
(en)

1976-07-28

FR2143142A1
(en)

1973-02-02

NL7204806A
(en)

1972-12-27

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Legal Events

Date
Code
Title
Description

1975-04-03
PS
Patent sealed [section 19, patents act 1949]

1983-01-19
PCNP
Patent ceased through non-payment of renewal fee

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