WO2012017447A3 - Method for selective hydration of aroma olefins to alcohols in continuous solid catalyst column reactor - Google Patents
Method for selective hydration of aroma olefins to alcohols in continuous solid catalyst column reactor Download PDFInfo
- Publication number
- WO2012017447A3 WO2012017447A3 PCT/IN2011/000493 IN2011000493W WO2012017447A3 WO 2012017447 A3 WO2012017447 A3 WO 2012017447A3 IN 2011000493 W IN2011000493 W IN 2011000493W WO 2012017447 A3 WO2012017447 A3 WO 2012017447A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- aroma
- column reactor
- olefins
- alcohols
- solid catalyst
- 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
- C07C29/03—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
- C07C29/04—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Present invention is related to method for selective hydration of aroma olefins to alcohols in continuous solid catalyst column reactor. The invention discloses the continuous production of unsaturated aroma alcohol and/or ester comprising of C10-12 carbon chain by selective solid acid catalyzed hydration reaction. According to the process of the invention production of Octa-1-ene-7- ol, 3,7-dimethyl- (Dihydromyrcenol) and/or dihydromyrcenyl acetate can be carried out by passing 1,6-Octadiene, 3,7-dimethyl- (dihydromyrcene) and water continuously through a packed bed column reactor wherein the residence time of column is not more than 90 minutes and reaction temperature not substantially above 100 degree C. The present disclosure solves the problem of effluent treatment and increases the yield of the process due to selectivity in reaction.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2211MU2010 | 2010-08-04 | ||
IN2211/MUM/2010 | 2010-08-04 |
Publications (3)
Publication Number | Publication Date |
---|---|
WO2012017447A2 WO2012017447A2 (en) | 2012-02-09 |
WO2012017447A8 WO2012017447A8 (en) | 2012-05-10 |
WO2012017447A3 true WO2012017447A3 (en) | 2012-06-07 |
Family
ID=44764194
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IN2011/000493 WO2012017447A2 (en) | 2010-08-04 | 2011-07-26 | Method for selective hydration of aroma olefins to alcohols in continuous solid catalyst column reactor |
Country Status (1)
Country | Link |
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WO (1) | WO2012017447A2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104926610B (en) * | 2015-05-27 | 2016-09-07 | 广西梧松林化集团有限公司 | The preparation method of dihydromyrcenol |
US11008271B2 (en) * | 2016-09-08 | 2021-05-18 | P2 Science, Inc. | Methods for the continuous alkoxylation and derivatization of terpenes |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101684065A (en) * | 2009-07-21 | 2010-03-31 | 厦门中坤化学有限公司 | Efficient energy-saving process for continuously processing dihydromyrcenol |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL113984C (en) | 1956-04-09 | |||
US3487118A (en) | 1966-10-17 | 1969-12-30 | Int Flavors & Fragrances Inc | Preparation of dihydromyrcenol |
GB1506131A (en) | 1976-02-04 | 1978-04-05 | Shell Bv | Preparation of dihydromyrcenol or a carboxylic ester thereof |
US4791222A (en) | 1984-07-31 | 1988-12-13 | International Flavors & Fragrances Inc. | Process for preparing dihydromyrcenol and dihydromyrcenyl acetate |
FR2597861B1 (en) | 1986-04-29 | 1990-11-09 | Derives Resiniques Terpenique | NEW PROCESS FOR THE PREPARATION OF DIHYDROMYRCENOL |
DE4021578A1 (en) | 1990-07-06 | 1992-01-09 | Huels Chemische Werke Ag | METHOD FOR PRODUCING DIHYDROMYRCENOL FROM DIHYDROMYRCENYL CHLORIDE |
ES2143281T3 (en) | 1996-01-15 | 2000-05-01 | Quest Int | TRANSESTERIFICATION PROCEDURE FOR THE PREPARATION OF DIHIDROMIRCENOL AND MIRCENOL. |
-
2011
- 2011-07-26 WO PCT/IN2011/000493 patent/WO2012017447A2/en active Application Filing
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101684065A (en) * | 2009-07-21 | 2010-03-31 | 厦门中坤化学有限公司 | Efficient energy-saving process for continuously processing dihydromyrcenol |
Non-Patent Citations (1)
Title |
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DATABASE WPI Week 201029, Derwent World Patents Index; AN 2010-E07057, XP002663149 * |
Also Published As
Publication number | Publication date |
---|---|
WO2012017447A8 (en) | 2012-05-10 |
WO2012017447A2 (en) | 2012-02-09 |
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