RU94045865A - Способ получения замещенных акролеинов, непрерывный способ альдольной конденсации альдегида и смесь с10-замещенных акролеинов - Google Patents

Способ получения замещенных акролеинов, непрерывный способ альдольной конденсации альдегида и смесь с10-замещенных акролеинов

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RU94045865A
RU94045865A RU94045865/04A RU94045865A RU94045865A RU 94045865 A RU94045865 A RU 94045865A RU 94045865/04 A RU94045865/04 A RU 94045865/04A RU 94045865 A RU94045865 A RU 94045865A RU 94045865 A RU94045865 A RU 94045865A
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acroleines
aldehyde
substituted
aldol condensation
catalyst solution
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RU94045865/04A
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RU2113429C1 (ru
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Эдвин Харрисон Джордж
Gb]
Джеймс Ризон Артур
Джеймс Деннис Элан
Шариф Мохаммад
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Деви Проссез Текнолоджи Лимитед (GB)
Деви Проссез Текнолоджи Лимитед
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/65Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups
    • C07C45/66Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups by dehydration
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
    • C07C45/74Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups combined with dehydration
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • C07C45/81Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • C07C45/81Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
    • C07C45/82Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Glass Compositions (AREA)
  • Iron Core Of Rotating Electric Machines (AREA)

Abstract

Альдольную конденсацию и дегидрацию проводят в реакторе с мешалкой 16, используя щелочной катализатор, такой как гидроксид натрия. Поток продукта реакции 23, содержащий как органическую, так и водную фазы, перегоняют (в колонке 25), получая гетерогенный азестроп, содержащий воду и альдегид. При конденсации и разделении фаз нижний водяной слой 34 может быть выражен из установки без необходимости проведения нейтрализации. Из нижней области дистилляционной зоны получают смесь 36 замещенного акролеина и раствора щелочного катализатора. Замещенный акролеин извлекают в качестве продукта 45, тогда как раствор катализатора 47 возвращают обратно в реактор альдольной конденсации. Часть 49 раствора катализатора удаляют, чтобы регулировать степень образования продуктов реакции Канниццаро.

Claims (1)

  1. Альдольную конденсацию и дегидрацию проводят в реакторе с мешалкой 16, используя щелочной катализатор, такой как гидроксид натрия. Поток продукта реакции 23, содержащий как органическую, так и водную фазы, перегоняют (в колонке 25), получая гетерогенный азестроп, содержащий воду и альдегид. При конденсации и разделении фаз нижний водяной слой 34 может быть выражен из установки без необходимости проведения нейтрализации. Из нижней области дистилляционной зоны получают смесь 36 замещенного акролеина и раствора щелочного катализатора. Замещенный акролеин извлекают в качестве продукта 45, тогда как раствор катализатора 47 возвращают обратно в реактор альдольной конденсации. Часть 49 раствора катализатора удаляют, чтобы регулировать степень образования продуктов реакции Канниццаро.
RU94045865A 1992-04-07 1993-04-07 Способ получения замещенных акролеинов RU2113429C1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB929207756A GB9207756D0 (en) 1992-04-07 1992-04-07 Process
GB9207756.9 1992-04-07

Publications (2)

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RU94045865A true RU94045865A (ru) 1996-08-10
RU2113429C1 RU2113429C1 (ru) 1998-06-20

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US (1) US5434313A (ru)
EP (2) EP0634994B1 (ru)
JP (1) JP3618099B2 (ru)
KR (1) KR100278134B1 (ru)
CN (1) CN1058697C (ru)
AT (1) ATE162169T1 (ru)
AU (1) AU659554B2 (ru)
BR (1) BR9306208A (ru)
CA (1) CA2133764A1 (ru)
DE (1) DE69316349T2 (ru)
ES (1) ES2114045T3 (ru)
FI (1) FI944619A (ru)
GB (1) GB9207756D0 (ru)
HU (1) HUT69744A (ru)
IN (1) IN181962B (ru)
MX (1) MX9302044A (ru)
NO (1) NO943694L (ru)
RO (1) RO117969B1 (ru)
RU (1) RU2113429C1 (ru)
SA (1) SA93130546B1 (ru)
SG (1) SG49573A1 (ru)
TW (1) TW241254B (ru)
WO (1) WO1993020034A1 (ru)
ZA (1) ZA932451B (ru)

Families Citing this family (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5667644A (en) * 1995-02-13 1997-09-16 Mitsubishi Chemical Corporation Method for producing a dimerized aldehyde
GB9519975D0 (en) * 1995-09-28 1995-11-29 Davy Process Techn Ltd Process
EP0838435A1 (en) 1996-10-25 1998-04-29 Kvaerner Process Technology Limited Process and plant for treating an aqueous waste stream containing alkali metal carboxylates
DE19956410A1 (de) * 1999-11-24 2001-05-31 Oxeno Olefinchemie Gmbh Verfahren zur Durchführung von Aldolkondensationen
US7335235B2 (en) 2002-04-26 2008-02-26 Basf Akiengesellschaft Alkoxylate mixtures and detergents containing the same
ES2342464T3 (es) * 2002-04-26 2010-07-07 Basf Se Mezclas de alcoxilatos de alcanol c sb 10 /sb y su aplicacion.
ATE388130T1 (de) 2002-04-26 2008-03-15 Basf Se C10-alkanolalkoxylate und ihre verwendung
DE10243366A1 (de) 2002-09-18 2004-04-01 Basf Ag Herstellung von Alkoxylaten bei optimierten Reaktionsdrücken
DE10249912A1 (de) 2002-10-26 2004-05-06 Oxeno Olefinchemie Gmbh Benzoesäureisodecyclestergemische, Herstellung und deren Verwendung
US6960694B2 (en) * 2003-07-01 2005-11-01 Eastman Chemical Company Processes for preparing β-hydroxy-ketones and α,β-unsaturated ketones
DE10348420A1 (de) * 2003-10-14 2005-05-25 Basf Ag C10-Alkanolalkoxylat-Gemische und ihre Verwendung - Neue schaumarme Netzer
US7071361B2 (en) * 2004-06-25 2006-07-04 Fastman Chemical Company Processes for the preparation of high molecular weight saturated ketones
ATE516376T1 (de) * 2004-12-24 2011-07-15 Basf Se Verwendung von nichtionischen tensiden bei der metallgewinnung
US7291748B2 (en) * 2005-07-28 2007-11-06 Basf Corporation C10/C7 ester mixtures based on 2-propylheptanol
AR064177A1 (es) * 2006-12-07 2009-03-18 Basf Ag Composiciones y kits que comprenden un triazol fungicida y un alcohol alcoxilado, y sus usos
DE502008001443D1 (de) * 2007-01-29 2010-11-11 Basf Se Verzweigte decylnitrate und ihre verwendung als verbrennungsverbesserer und/oder cetanzahlverbesserer in kraftstoffen
TW201031743A (en) 2008-12-18 2010-09-01 Basf Se Surfactant mixture comprising branched short-chain and branched long-chain components
DE102009001594A1 (de) 2009-03-17 2010-09-30 Evonik Oxeno Gmbh Verfahren zur Herstellung von alpha, beta-ungesättigten C10-Aldehyden
DE102009028976A1 (de) 2009-08-28 2011-03-03 Evonik Oxeno Gmbh Ester der 2,5-Furandicarbonsäure mit isomeren Decanolen und ihre Verwendung
DE102009045139A1 (de) 2009-09-30 2011-03-31 Evonik Oxeno Gmbh Herstellung von alpha,beta-ungesättigten Aldehyden mittels einer Reaktionsmischpumpe
EP2496654B1 (de) 2009-11-05 2014-04-02 Basf Se Kleb- und dichtstoffe enthaltend ester auf basis von 2-propylheptanol
ES2525017T3 (es) 2010-08-03 2014-12-16 Basf Se Líquidos portadores para abrasivos
WO2012084914A1 (de) 2010-12-23 2012-06-28 Basf Se Thermoplastische elastomer-zusammensetzung und verfahren zu deren herstellung
DE102011121087A1 (de) 2011-12-14 2013-06-20 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Verfahren zur katalytischen Kondensation oder Kopplung
US8742177B2 (en) * 2011-12-28 2014-06-03 Rohm And Haas Company Catalyst and process to produce branched unsaturated aldehydes
JP2015505574A (ja) 2012-02-01 2015-02-23 ビーエーエスエフ ソシエタス・ヨーロピアBasf Se ウェハ製造のための冷却および/または潤滑液
US9006495B2 (en) 2012-11-30 2015-04-14 Basf Se Process for the catalytic aldol condensation of aldehydes
PL2925714T3 (pl) 2012-11-30 2017-05-31 Basf Se Sposób katalitycznej kondensacji aldolowej aldehydów
TWI654177B (zh) 2013-10-31 2019-03-21 德商巴斯夫歐洲公司 製備羧酸酯的方法及其作爲塑化劑的用途
PL3077453T3 (pl) 2013-12-06 2018-10-31 Basf Se Kompozycja plastyfikatora zawierająca pochodne tetrahydrofuranu i estry kwasu 1,2-cykloheksanodikarboksylowego
KR20160106657A (ko) 2014-01-09 2016-09-12 바스프 에스이 푸란 유도체 및 1,2-시클로헥산디카르복실산 에스테르를 함유하는 가소제 조성물
KR20160148611A (ko) 2014-04-22 2016-12-26 바스프 에스이 이온성 액체 및 산성 에스테르화 촉매의 존재 하의 카르복실산 에스테르의 제조 방법 및 가소제로서의 그 용도
DE102015207291A1 (de) 2014-04-24 2016-03-10 Basf Se Weichmacher-Zusammensetzung, die Furanderivate und 1,2-Cyclohexandicarbonsäureester enthält
FR3021314B1 (fr) * 2014-05-26 2016-05-13 Rhodia Operations Procede de preparation de composes p-hydroxymandeliques en reacteurs agites
TW201609628A (zh) 2014-07-08 2016-03-16 巴斯夫歐洲公司 包含脂族二羧酸二酯及對苯二甲酸二烷基酯之塑化劑組成物
TW201605945A (zh) 2014-07-08 2016-02-16 巴斯夫歐洲公司 包含二羧酸的酯及1,2-環己烷二羧酸的酯之模製化合物
TWI706979B (zh) 2014-08-19 2020-10-11 德商巴斯夫歐洲公司 包含聚合二羧酸酯的塑化劑組成物
TWI686444B (zh) 2014-09-04 2020-03-01 德商巴斯夫歐洲公司 包含聚合二羧酸酯的塑化劑組成物
DE202014007140U1 (de) 2014-09-08 2014-10-22 Basf Se Öl-basierte Bohrflüssigkeiten mit Copolymeren aus Styrol, (Meth)acrylaten von C10-Alkoholgemischen und (Meth)acrylsäure
DE202014007136U1 (de) 2014-09-08 2014-10-16 Basf Se Härtbare Zusammensetzung, hergestellt mit einem aus (Meth)acrylaten von C10-Alkoholgemischen aufgebauten Copolymer
TW201619119A (zh) 2014-10-09 2016-06-01 巴斯夫歐洲公司 包含飽和二羧酸之環烷基酯及1,2-環己烷二羧酸酯的塑化劑組成物
TW201619120A (zh) 2014-10-09 2016-06-01 巴斯夫歐洲公司 包含飽和二羧酸之環烷基酯及對苯二甲酯之塑化劑組成物
WO2016075070A1 (en) 2014-11-10 2016-05-19 Basf Se Ethylene-propylheptyl(meth-)acrylate copolymers
US10287417B2 (en) 2015-01-30 2019-05-14 Basf Se Plasticizer composition containing polymeric dicarboxylic acid esters and terephthalic acid dialkyl esters
RU2727926C9 (ru) 2015-09-30 2021-05-21 Басф Се Пластифицирующая композиция, содержащая полимерные сложные эфиры дикарбоновых кислот и сложные диэфиры дикарбоновых кислот
PL3356457T5 (pl) 2015-09-30 2023-04-24 Basf Se Kompozycja plastyfikatora zawierająca polimerowe estry kwasu dikarboksylowego i estry kwasu 1,2-cykloheksanodikarboksylowego
WO2017055432A1 (de) 2015-09-30 2017-04-06 Basf Se Weichmacher-zusammensetzung, die polymere dicarbonsäureester und terephthalsäuredialkylester enthält
RU2729055C2 (ru) 2016-01-20 2020-08-04 Басф Се Пластифицирующая композиция, которая содержит алифатический сложный эфир дикарбоновой кислоты и сложный диэфир, выбранный из сложных эфиров 1,2-циклогександикарбоновой кислоты и сложных эфиров терефталевой кислоты
CN109196034B (zh) 2016-03-23 2021-06-08 巴斯夫欧洲公司 包含环烷基烷基二羧酸二酯作为增塑剂的聚合物组合物
RU2019105682A (ru) 2016-08-01 2020-09-01 Басф Се Композиция пластификатора
WO2018024591A1 (de) 2016-08-01 2018-02-08 Basf Se Weichmacher-zusammensetzung
WO2018024597A1 (de) 2016-08-01 2018-02-08 Basf Se Weichmacher-zusammensetzung
EP3301084B1 (de) 2016-09-30 2018-12-12 OXEA GmbH Kontinuierliches herstellungsverfahren für 2-methylenalkanale
GB201617463D0 (en) 2016-10-14 2016-11-30 Johnson Matthey Davy Technologies Limited Process
JP7009511B2 (ja) * 2017-05-25 2022-02-10 ローム アンド ハース カンパニー メタクロレインを調製するためのプロセス
CN110809623B (zh) 2017-06-28 2022-09-06 陶氏环球技术有限责任公司 易于生物降解的烷氧基化物混合物
WO2019185409A1 (de) 2018-03-29 2019-10-03 Basf Se Pvc-zusammensetzung, enthaltend wenigstens einen weichmacher der wenigstens eine carbonsäureestergruppe aufweist und wenigstens eine carbodiimidverbindung
CN108658742B (zh) * 2018-04-27 2021-08-17 宿迁科思化学有限公司 一种铃兰醛关键中间体对叔丁基-α-甲基苯丙烯醛的制备方法
EP3747860B1 (de) 2019-06-04 2023-07-26 Basf Se Neue weichmacher auf cyclohexanon-basis
EP3786146A1 (de) * 2019-08-30 2021-03-03 Röhm GmbH Verfahren zur herstellung von methacrolein aus formaldehyd und propionaldehyd sowie herstellanlage hierfür
KR102675020B1 (ko) * 2019-10-08 2024-06-14 한화솔루션 주식회사 알돌 축합 반응 장치
CN116063167A (zh) * 2021-11-01 2023-05-05 中国石油化工股份有限公司 一种制备2-丙基-2-庚烯醛的方法及装置和所得2-丙基-2-庚烯醛
GB202213997D0 (en) 2022-09-26 2022-11-09 Johnson Matthey Davy Technologies Ltd Parallel zone hydroformylation reaction
CN117229132B (zh) * 2023-11-10 2024-02-20 济南悟通生物科技有限公司 一种反式-2,4-壬二烯醛的合成方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB549006A (en) * 1940-02-12 1942-11-03 Shell Dev Condensation of carbonylic compounds
FR1036156A (fr) * 1951-04-25 1953-09-04 Melle Usines Sa Procédé de préparation d'aldéhydes aliphatiques non saturées
GB1010695A (en) * 1961-12-22 1965-11-24 Exxon Research Engineering Co Process for the production of alpha, beta unsaturated carbonyl compounds
US3248428A (en) * 1961-12-22 1966-04-26 Exxon Research Engineering Co Aldolization process
DE3106557A1 (de) * 1981-02-21 1982-09-16 Basf Ag, 6700 Ludwigshafen Verfahren zur herstellung von (alpha)-alkylacroleinen
DE3740293A1 (de) * 1987-11-27 1989-06-01 Hoechst Ag Verfahren zur herstellung von alpha-alkylacroleinen
CA2068489A1 (en) * 1991-05-16 1992-11-17 Masaru Ishino Aldol condensation dehydration catalyst, a process for preparing the same and a process for preparing an aldol condensation dehydrate using the process

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RO117969B1 (ro) 2002-11-29
IN181962B (ru) 1998-11-21
SA93130546B1 (ar) 2004-08-29
JPH07505390A (ja) 1995-06-15
EP0751109A1 (en) 1997-01-02
RU2113429C1 (ru) 1998-06-20
ES2114045T3 (es) 1998-05-16
DE69316349T2 (de) 1998-07-23
KR950700869A (ko) 1995-02-20
TW241254B (ru) 1995-02-21
FI944619A0 (fi) 1994-10-04
AU659554B2 (en) 1995-05-18
GB9207756D0 (en) 1992-05-27
CN1105012A (zh) 1995-07-12
AU3958793A (en) 1993-11-08
JP3618099B2 (ja) 2005-02-09
CN1058697C (zh) 2000-11-22
HUT69744A (en) 1995-09-28
US5434313A (en) 1995-07-18
KR100278134B1 (ko) 2001-02-01
MX9302044A (es) 1994-07-29
ZA932451B (en) 1993-10-20
ATE162169T1 (de) 1998-01-15
WO1993020034A1 (en) 1993-10-14
NO943694L (no) 1994-12-06
NO943694D0 (no) 1994-10-04
CA2133764A1 (en) 1993-10-14
EP0634994A1 (en) 1995-01-25
EP0634994B1 (en) 1998-01-14
BR9306208A (pt) 1998-06-23
FI944619A (fi) 1994-10-04
SG49573A1 (en) 1998-06-15
DE69316349D1 (de) 1998-02-19

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