IN2014DN08906A - - Google Patents
Info
- Publication number
- IN2014DN08906A IN2014DN08906A IN8906DEN2014A IN2014DN08906A IN 2014DN08906 A IN2014DN08906 A IN 2014DN08906A IN 8906DEN2014 A IN8906DEN2014 A IN 8906DEN2014A IN 2014DN08906 A IN2014DN08906 A IN 2014DN08906A
- Authority
- IN
- India
- Prior art keywords
- unsaturated alcohol
- hydrocarby
- fuels
- organic solvent
- unsaturated
- 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
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/147—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
-
- 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
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/02—Preparation of ethers from oxiranes
- C07C41/03—Preparation of ethers from oxiranes by reaction of oxirane rings with hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/05—Preparation of ethers by addition of compounds to unsaturated compounds
- C07C41/06—Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/178—Unsaturated ethers containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/007—Esters of unsaturated alcohols having the esterified hydroxy group bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F216/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an alcohol radical
- C08F216/04—Acyclic compounds
Abstract
Unsaturated alcohol compositions are obtained by reducing a metathesis derived hydrocarby! unsaturated ester. Also disclosed is a process for preparing an unsaturated alcohol composition where a metathesis derived hydrocarby! carbonyl compound is reacted in the presence of a silane compound an organic solvent and a catalyst system prepared from a metallic complex and a reducing agent. This mixture is then hydrolyzed with a metallic base and then mixed with organic solvent. The resultant mixture is then separated washed dried and/or purified to produce the unsaturated alcohol composition. The unsaturated alcohol derivatives are useful in many end use applications including for example lubricants functional fluids fuels functional additives for such lubricants functional fluids and fuels plasticizers asphalt additives friction reducing agents plastics and adhesives.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261637574P | 2012-04-24 | 2012-04-24 | |
US201361780490P | 2013-03-13 | 2013-03-13 | |
PCT/US2013/037568 WO2013163071A1 (en) | 2012-04-24 | 2013-04-22 | Unsaturated fatty alcohol compositions and derivatives from natural oil metathesis |
Publications (1)
Publication Number | Publication Date |
---|---|
IN2014DN08906A true IN2014DN08906A (en) | 2015-05-22 |
Family
ID=48289654
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IN8906DEN2014 IN2014DN08906A (en) | 2012-04-24 | 2013-04-22 |
Country Status (6)
Country | Link |
---|---|
US (2) | US20130281688A1 (en) |
EP (1) | EP2841407A1 (en) |
CN (1) | CN104271542A (en) |
CA (1) | CA2871428A1 (en) |
IN (1) | IN2014DN08906A (en) |
WO (1) | WO2013163071A1 (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10745347B2 (en) | 2012-04-24 | 2020-08-18 | Stepan Company | Unsaturated fatty alcohol derivatives from natural oil metathesis |
AU2013252874B2 (en) | 2012-04-24 | 2016-04-21 | Stepan Company | Unsaturated fatty alcohol alkoxylates from natural oil metathesis |
WO2015108874A1 (en) * | 2014-01-16 | 2015-07-23 | Elevance Renewable Sciences, Inc. | Olefinic ester compositions and their use in oil- and gas-related applications |
US10081760B2 (en) | 2014-01-16 | 2018-09-25 | Elevance Renewable Sciences, Inc. | Olefinic ester compositions and their use in stimulating hydrocarbon production from a subterranean formation |
US11053430B2 (en) | 2014-01-16 | 2021-07-06 | Wilmar Trading Pte Ltd. | Olefinic ester compositions and their use in stimulating hydrocarbon production from a subterranean formation |
US10759990B2 (en) | 2014-01-16 | 2020-09-01 | Wilmar Trading Pte Ltd. | Use of olefinic ester compositions in oil and gas fields |
ES2590220B1 (en) | 2015-05-18 | 2017-12-18 | Neol Biosolutions, S.A. | PRODUCTION OF MICROBIAL OILS WITH HIGH CONTENT IN OIL ACID |
CA3005562A1 (en) | 2015-11-18 | 2017-05-26 | Provivi, Inc. | Production of fatty olefin derivatives via olefin metathesis |
JP6737885B2 (en) | 2015-11-18 | 2020-08-12 | プロヴィヴィ インコーポレイテッド | Microorganisms and related compounds for the production of insect pheromones |
CA3012433C (en) | 2016-03-04 | 2020-04-28 | Halliburton Energy Services, Inc. | Improved performance non-emulsifiers that employ branched alcohols and a new high-solvency carrier oil |
WO2017151159A1 (en) | 2016-03-04 | 2017-09-08 | Halliburton Energy Services, Inc. | Alkyl unsaturated fatty acid ester oil as a oil component in the formulation and application of surfactant flowback aids for subterranean stimulation |
JP2019517797A (en) * | 2016-06-06 | 2019-06-27 | プロヴィヴィ インコーポレイテッド | Semibiosynthetic production of fatty alcohols and fatty aldehydes |
US20180049970A1 (en) * | 2016-08-18 | 2018-02-22 | The Procter & Gamble Company | Hair care compositions comprising metathesized unsaturated polyol esters |
EP3583088A4 (en) | 2017-02-17 | 2021-03-31 | Provivi, Inc. | Synthesis of pheromones and related materials via olefin metathesis |
CN110914442A (en) | 2017-05-17 | 2020-03-24 | 普罗维维股份有限公司 | Microorganisms for the production of insect pheromones and related compounds |
CN109231893A (en) * | 2018-10-19 | 2019-01-18 | 湖北津泰环保科技有限公司 | A kind of stone mastic asphalt and preparation method thereof that anti-time property is good |
CN110170077B (en) * | 2019-03-26 | 2021-09-28 | 南京理工大学 | Polyion type biological lubricant and preparation method thereof |
BR112022023772A2 (en) * | 2020-06-01 | 2022-12-20 | Provivi Inc | SYNTHESIS OF PHEROMONE DERIVATIVES BY Z-SELECTIVE OLEFIN METATHESIS |
CN116568787A (en) * | 2020-12-08 | 2023-08-08 | 联合利华知识产权控股有限公司 | Oleyl alcohol and method of production |
Family Cites Families (32)
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US2865968A (en) | 1955-05-06 | 1958-12-23 | Nat Distillers Chem Corp | Production of fatty alcohols |
DE965236C (en) | 1955-08-22 | 1957-06-06 | Dehydag Gmbh | Process for the continuous production of simply unsaturated, higher molecular weight fatty alcohols |
US4545941A (en) * | 1983-06-20 | 1985-10-08 | A. E. Staley Manufacturing Company | Co-metathesis of triglycerides and ethylene |
US4804790A (en) | 1983-07-14 | 1989-02-14 | Henkel Kommanditgesellschaft Auf Aktien | Process for obtaining fatty alcohols from free fatty acids |
DE3724254A1 (en) | 1987-07-22 | 1989-02-02 | Henkel Kgaa | METHOD FOR HYDROGENATING FATTY ACID METHYL ESTERS IN THE PRESSURE RANGE FROM 20 TO 100 BAR |
DE4142515A1 (en) * | 1991-12-21 | 1993-06-24 | Basf Ag | METHOD FOR PRODUCING ALKENOLS |
EP0773948A4 (en) | 1992-04-03 | 1998-09-02 | California Inst Of Techn | High activity ruthenium or osmium metal carbene complexes for olefin metathesis reactions and synthesis thereof |
US5710298A (en) | 1992-04-03 | 1998-01-20 | California Institute Of Technology | Method of preparing ruthenium and osmium carbene complexes |
US5312940A (en) | 1992-04-03 | 1994-05-17 | California Institute Of Technology | Ruthenium and osmium metal carbene complexes for olefin metathesis polymerization |
DE4242466C2 (en) | 1992-12-16 | 2003-07-03 | Cognis Deutschland Gmbh | Process for the production of fatty alcohols |
DE4335781C2 (en) | 1993-10-20 | 1998-02-19 | Henkel Kgaa | Vegetable-based fatty alcohols and process for their preparation |
DE4422858C1 (en) | 1994-06-30 | 1995-07-27 | Henkel Kgaa | Unsatd. fatty alcohol(s) with improved low-temp. properties |
JP3004361B2 (en) | 1994-10-19 | 2000-01-31 | フイルメニツヒ ソシエテ アノニム | Method for producing alcohol |
US6683224B1 (en) | 1995-05-03 | 2004-01-27 | Cognis Deutschland Gmbh & Co. Kg | Process for the production of fatty alcohols |
US5728785A (en) | 1995-07-07 | 1998-03-17 | California Institute Of Technology | Romp polymerization in the presence of peroxide crosslinking agents to form high-density crosslinked polymers |
US5831108A (en) | 1995-08-03 | 1998-11-03 | California Institute Of Technology | High metathesis activity ruthenium and osmium metal carbene complexes |
CN1222903A (en) * | 1996-04-24 | 1999-07-14 | 联合碳化化学品及塑料技术公司 | Processes for producing hydroxyaldehydes |
DE19750800C2 (en) | 1997-11-17 | 2001-04-26 | Cognis Deutschland Gmbh | Process for the production of unsaturated palm fatty alcohols |
DE19815275B4 (en) | 1998-04-06 | 2009-06-25 | Evonik Degussa Gmbh | Alkylidene complexes of ruthenium with N-heterocyclic carbene ligands and their use as highly active, selective catalysts for olefin metathesis |
US6159928A (en) * | 1998-04-13 | 2000-12-12 | Kuraray Co., Ltd. | Cis-configurational unsaturated ester, process for producing the same, and fragrance composition containing the same |
US6696597B2 (en) | 1998-09-01 | 2004-02-24 | Tilliechem, Inc. | Metathesis syntheses of pheromones or their components |
CA2361148C (en) | 1999-01-26 | 2009-06-30 | California Institute Of Technology | Novel methods for cross-metathesis of terminal olefins |
AU2001271430B2 (en) | 2000-06-23 | 2006-09-07 | California Institute Of Technology | Synthesis of functionalized and unfunctionalized olefins via cross and ring-closing metathesis |
US6594947B2 (en) * | 2001-10-17 | 2003-07-22 | Trece, Inc. | Multi-component device for capturing or repelling insects or insect pests |
JP4034289B2 (en) | 2004-04-02 | 2008-01-16 | 花王株式会社 | Method for producing fatty alcohol |
US7592497B2 (en) | 2006-03-24 | 2009-09-22 | Exxonmobil Chemical Patents Inc. | Low viscosity polyalphapolefin based on 1-decene and 1-dodecene |
US7544850B2 (en) | 2006-03-24 | 2009-06-09 | Exxonmobil Chemical Patents Inc. | Low viscosity PAO based on 1-tetradecene |
CN106083579A (en) * | 2006-10-13 | 2016-11-09 | 埃莱文斯可更新科学公司 | By olefin metathesis by the method for internal olefin synthesis terminal olefin |
EP2121546B1 (en) | 2006-10-13 | 2017-12-13 | Elevance Renewable Sciences, Inc. | Methods of making alpha, omega-dicarboxylic acid alkene derivatives by metathesis |
WO2008048522A1 (en) | 2006-10-13 | 2008-04-24 | Elevance Renewable Sciences, Inc. | Methods of making monounsaturated functionalized alkene compounds by metathesis |
CN101802097B (en) * | 2007-08-02 | 2012-11-14 | 科莱恩金融(Bvi)有限公司 | Phosphoric acid esters containing phosphorus atoms bridged by diol units |
CN102770520B (en) | 2009-10-12 | 2014-12-17 | 艾勒旺斯可再生科学公司 | Methods of refining and producing fuel from natural oil feedstocks |
-
2013
- 2013-04-22 IN IN8906DEN2014 patent/IN2014DN08906A/en unknown
- 2013-04-22 US US13/867,542 patent/US20130281688A1/en not_active Abandoned
- 2013-04-22 CN CN201380021877.2A patent/CN104271542A/en active Pending
- 2013-04-22 WO PCT/US2013/037568 patent/WO2013163071A1/en active Application Filing
- 2013-04-22 EP EP13720672.8A patent/EP2841407A1/en not_active Withdrawn
- 2013-04-22 CA CA2871428A patent/CA2871428A1/en not_active Abandoned
-
2015
- 2015-06-12 US US14/738,493 patent/US20150274619A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
CA2871428A1 (en) | 2013-10-31 |
WO2013163071A1 (en) | 2013-10-31 |
US20130281688A1 (en) | 2013-10-24 |
EP2841407A1 (en) | 2015-03-04 |
US20150274619A1 (en) | 2015-10-01 |
CN104271542A (en) | 2015-01-07 |
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