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KR910016676A - α,β-불포화카르복시산 에스테르의 제조 방법 - Google Patents

α,β-불포화카르복시산 에스테르의 제조 방법 Download PDF

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Publication number
KR910016676A
KR910016676A KR1019910003960A KR910003960A KR910016676A KR 910016676 A KR910016676 A KR 910016676A KR 1019910003960 A KR1019910003960 A KR 1019910003960A KR 910003960 A KR910003960 A KR 910003960A KR 910016676 A KR910016676 A KR 910016676A
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South Korea
Prior art keywords
acid ester
unsaturated carboxylic
carboxylic acid
catalyst
producing
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KR1019910003960A
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KR960000042B1 (ko
Inventor
요시까즈 시마
다까후미 아베
히로후미 히구찌
고이찌 기다
Original Assignee
니시까오 레이지
미쓰비시 가스가가꾸 가부시끼가이샤
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Publication of KR910016676A publication Critical patent/KR910016676A/ko
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Publication of KR960000042B1 publication Critical patent/KR960000042B1/ko

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/52Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
    • C07C69/587Monocarboxylic acid esters having at least two carbon-to-carbon double bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/317Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
    • C07C67/327Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups by elimination of functional groups containing oxygen only in singly bound form

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)

Abstract

내용 없음

Description

α,β-불포화카르복시산 에스테르의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (7)

  1. α-히드록시카르복시산에스테르를 결정성 알루미노규산염에 촉매에 접촉반응시키고, 이어서 얻어진 반응생성물을 고체산촉매로 접촉시키는 것을 특징으로 하는 α, β-불포화카르복시산에스테르의 제조방법.
  2. 제1항에 있어서, 결정성 알루미노규산염이 X형 제올라이트 또는 Y형 제올라이트인 α, β-불포화카르복시산에스테르의 제조방법.
  3. 제1항에 있어서, 고체산촉매가 인산염을 함유하는 촉매, 고체인산촉매, 황산염을 함유하는 촉매, 실리카-알루미나, 실리카-티타니아, 실리카-지르코니아 또는 제올라이트인 α, β-불포화카르복시산에스테르의 제조방법.
  4. 제1항에 있어서, α-히드록시카르복시산에스테르가, α-히드록시이소부티르산메틸 및 락트산메틸인 α, β-불포화카르복시산에스테르의 제조방법.
  5. 제1항에 있어서, 원료인 α-히드록시카르복시산에스테르의 알콕시부분에 상당하는 알코올을 반응용매로서 사용하는 α,β-불포화카르복시산에스테르의 제조방법.
  6. 제1항에 있어서, 반응용매로서 알코올을 α-히드록시카르복시산에스테르에 대하여 1-10배몰의 범위로 사용하는 α, β-불포화카르복시산에스테르의 제조방법.
  7. 제1항에 있어서, 결정성 알루미노규산염촉매와의 접촉반응시의 온도가 150-450℃이며, 고체산촉매와의 접촉반응시의 온도가 50-450℃인 α, β-불포화카르복시산에스테르의 제조방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019910003960A 1990-03-15 1991-03-13 α, β-불포화카르복시산에스테르의 제조방법 KR960000042B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP62751/1990 1990-03-15
JP2062751A JP2906547B2 (ja) 1990-03-15 1990-03-15 α,β―不飽和カルボン酸エステルの製造方法

Publications (2)

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KR910016676A true KR910016676A (ko) 1991-11-05
KR960000042B1 KR960000042B1 (ko) 1996-01-03

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KR1019910003960A KR960000042B1 (ko) 1990-03-15 1991-03-13 α, β-불포화카르복시산에스테르의 제조방법

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US (1) US5075493A (ko)
EP (1) EP0446446B1 (ko)
JP (1) JP2906547B2 (ko)
KR (1) KR960000042B1 (ko)
DE (1) DE69013490T2 (ko)
ES (1) ES2065462T3 (ko)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3189858B2 (ja) * 1992-11-16 2001-07-16 三菱瓦斯化学株式会社 メタクリル酸メチルの製造法
EP0768296B1 (en) * 1995-10-10 2001-06-13 Rohm And Haas Company A method for making alpha, beta-unsaturated-beta-trifluoromethyl-carboxylates
EP1186592A1 (en) * 2000-09-11 2002-03-13 Mitsubishi Gas Chemical Company, Ltd. Production of methacrylates
JP4810770B2 (ja) * 2001-07-18 2011-11-09 三菱瓦斯化学株式会社 メタクリル酸アリルの製造方法
WO2005095320A1 (en) * 2004-04-02 2005-10-13 Ciba Specialty Chemicals Water Treatments Limited Preparation of acrylic acid derivatives from alpha or beta-hydroxy carboxylic acids
JP6694641B2 (ja) * 2015-06-30 2020-05-20 国立研究開発法人産業技術総合研究所 アクリル酸等のα、β−不飽和カルボン酸、その誘導体の製造法
EP4452919A1 (de) 2021-12-23 2024-10-30 Röhm GmbH Verfahren zur herstellung von alkylmethacrylaten mit verbesserter ausbeute und verminderten emissionen flüchtiger organischer verbindungen
WO2023169810A1 (de) 2022-03-11 2023-09-14 Röhm Gmbh Verfahren zur herstellung von alpha-hydroxyisobuttersäuremethylester und dessen anwendung in der elektronik-industrie

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2376704A (en) * 1943-10-01 1945-05-22 Goodrich Co B F Preparation of esters of alpha-beta unsaturated monocarboxylic acids
US2485510A (en) * 1946-02-13 1949-10-18 American Cyanamid Co Preparation of acrylic acid and esters thereof
DE1211153B (de) * 1957-10-29 1966-02-24 Escambia Chem Corp Verfahren zur Herstellung von Methacrylsaeure und bzw. oder deren Estern durch Umsetzung der Daempfe von alpha-Oxyisobuttersaeure oder deren Estern
US3022337A (en) * 1958-06-03 1962-02-20 Wacker Chemie Gmbh Process for the catalytic production of unsaturated mono-carboxylic acid esters
JPS5767534A (en) * 1980-10-16 1982-04-24 Mitsui Toatsu Chem Inc Preparation of alpha,beta-unsaturated carboxylic ester and alpha,beta-unsaturated carboxylic acid
US4812593A (en) * 1986-08-27 1989-03-14 Basf Aktiengesellschaft Preparation of bifunctional compounds
JPH0727519B2 (ja) * 1987-10-09 1995-03-29 株式会社日立製作所 数式編集方式
JP2727618B2 (ja) * 1989-01-26 1998-03-11 三菱瓦斯化学株式会社 不飽和カルボン酸エステルの製造方法

Also Published As

Publication number Publication date
DE69013490T2 (de) 1995-03-23
JP2906547B2 (ja) 1999-06-21
KR960000042B1 (ko) 1996-01-03
JPH03264548A (ja) 1991-11-25
ES2065462T3 (es) 1995-02-16
EP0446446A3 (en) 1992-03-04
EP0446446A2 (en) 1991-09-18
DE69013490D1 (de) 1994-11-24
US5075493A (en) 1991-12-24
EP0446446B1 (en) 1994-10-19

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