CH412858A - Process for the production of polyolefinic alcohols - Google Patents
Process for the production of polyolefinic alcoholsInfo
- Publication number
- CH412858A CH412858A CH1486861A CH1486861A CH412858A CH 412858 A CH412858 A CH 412858A CH 1486861 A CH1486861 A CH 1486861A CH 1486861 A CH1486861 A CH 1486861A CH 412858 A CH412858 A CH 412858A
- Authority
- CH
- Switzerland
- Prior art keywords
- group
- alkyl group
- carbon atoms
- methyl group
- optional
- Prior art date
Links
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
- C07C29/09—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
- C07C29/095—Preparation 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/16—Preparation of halogenated hydrocarbons by replacement by halogens of hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C33/02—Acyclic alcohols with carbon-to-carbon double bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/10—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with ester groups or with a carbon-halogen bond
- C07C67/11—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with ester groups or with a carbon-halogen bond being mineral ester groups
-
- 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
-
- 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
- C11B9/0007—Aliphatic 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
- C11B9/0007—Aliphatic compounds
- C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
-
- 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
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
- C12C11/00—Fermentation processes for beer
- C12C11/02—Pitching yeast
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Food Science & Technology (AREA)
- Zoology (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises compounds of the general formula: <FORM:0960756/C1/1> in which the broken lines denote optional bonds, R1 is a phenyl group or an alkyl group containing 2-4 carbon atoms in the case of trienes in which the optional methyl group is absent and/or otherwise an alkyl group containing 1-4 carbon atoms, and R2 is a methyl group or together with R1 a pentamethylene group. They are prepared by halogenating an alcohol of formula: <FORM:0960756/C1/2> by known methods to replace the OH group by a halogen atom with allyl rearrangement, converting the product by treatment with an inorganic salt of an alkane carboxylic acid containing 1-5 carbon atoms into a carboxylic ester and hydrolyzing the ester with an aqueous alcoholic solution of an inorganic base. Preferred tertiary alcohol starting materials are 3, 7, 11-trimethyl-tridecatrien-(1, 6, 10)-ol-13), 3, 7, 10, 11-tetramethyl-dodcecatrien-(1, 6, 10)-ol-(3) and 3, 7, 11-trimethyl-dodcecadien-(1,6)-ol-(3). The halogenation may be carried out by treating the tertiary alcohol with concentrated aqueous hydrochloric or hydrobromic acid, phosphorus tribromide or anhydrous hydrogen chloride or bromide. The halogenation is accompanied by an allyl rearrangement resulting in the formation of 1-halo compounds.ALSO:Alcohols of general formula <FORM:0960756/A5-A6/1> in which the broken lines denote optional bonds, R1 is a phenyl group or a C2-C4 alkyl group in the case of trienes in which the optional methyl group is absent but otherwise a C1-C4 alkyl group and R2 is a methyl group or, together with R1 a pentamethylene group, may be used as insecticidal ingredients in mixtures for combating insects. They may be used in admixture with other insecticides and in emulsions, suspension, dusts, solutions or aerosol sprays.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL286966D NL286966A (en) | 1961-12-22 | ||
CH1486861A CH412858A (en) | 1961-12-22 | 1961-12-22 | Process for the production of polyolefinic alcohols |
DEH47573A DE1191365B (en) | 1961-12-22 | 1962-12-03 | Process for the production of polyolefinic alcohols |
FR918904A FR1344638A (en) | 1961-12-22 | 1962-12-18 | Process for the preparation of polyolefin alcohols |
GB48080/62A GB960756A (en) | 1961-12-22 | 1962-12-20 | Novel unsaturated alcohols and a process for the manufacture thereof |
BE625929A BE625929A (en) | 1961-12-22 | 1963-06-11 | Process for the preparation of polyolefin alcohols |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1486861A CH412858A (en) | 1961-12-22 | 1961-12-22 | Process for the production of polyolefinic alcohols |
Publications (1)
Publication Number | Publication Date |
---|---|
CH412858A true CH412858A (en) | 1966-05-15 |
Family
ID=4404431
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH1486861A CH412858A (en) | 1961-12-22 | 1961-12-22 | Process for the production of polyolefinic alcohols |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE625929A (en) |
CH (1) | CH412858A (en) |
DE (1) | DE1191365B (en) |
FR (1) | FR1344638A (en) |
GB (1) | GB960756A (en) |
NL (1) | NL286966A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4292454A (en) | 1977-12-29 | 1981-09-29 | Scm Corporation | Coupling reaction involving a Grignard and allylic halide |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH360384A (en) * | 1956-07-30 | 1962-02-28 | Hoffmann La Roche | Process for the production of polyolefinic alcohols |
-
0
- NL NL286966D patent/NL286966A/xx unknown
-
1961
- 1961-12-22 CH CH1486861A patent/CH412858A/en unknown
-
1962
- 1962-12-03 DE DEH47573A patent/DE1191365B/en active Pending
- 1962-12-18 FR FR918904A patent/FR1344638A/en not_active Expired
- 1962-12-20 GB GB48080/62A patent/GB960756A/en not_active Expired
-
1963
- 1963-06-11 BE BE625929A patent/BE625929A/en unknown
Also Published As
Publication number | Publication date |
---|---|
FR1344638A (en) | 1963-11-29 |
BE625929A (en) | 1963-06-11 |
DE1191365B (en) | 1965-04-22 |
NL286966A (en) | |
GB960756A (en) | 1964-06-17 |
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