ES2034701T3 - Procedimiento perfeccionado para la fabricacion de metacrilato de metilo a partir del acido isobutirico. - Google Patents

Procedimiento perfeccionado para la fabricacion de metacrilato de metilo a partir del acido isobutirico.

Info

Publication number
ES2034701T3
ES2034701T3 ES198989402286T ES89402286T ES2034701T3 ES 2034701 T3 ES2034701 T3 ES 2034701T3 ES 198989402286 T ES198989402286 T ES 198989402286T ES 89402286 T ES89402286 T ES 89402286T ES 2034701 T3 ES2034701 T3 ES 2034701T3
Authority
ES
Spain
Prior art keywords
manufacture
methyl methacrylate
isobutyric acid
perfected procedure
perfected
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES198989402286T
Other languages
English (en)
Inventor
Yves Samuel
Daniel Cauvy
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Arkema France SA
Original Assignee
Elf Atochem SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Elf Atochem SA filed Critical Elf Atochem SA
Application granted granted Critical
Publication of ES2034701T3 publication Critical patent/ES2034701T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
    • C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
    • C07C69/54—Acrylic acid esters; Methacrylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/48—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/377—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional 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
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/48—Separation; Purification; Stabilisation; Use of additives
    • C07C67/58—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Fats And Perfumes (AREA)
  • Saccharide Compounds (AREA)

Abstract

SE SOMETE EL ACIDO ISOBUTIRICO A UNA OXIDESHIDROGENACION CATALITICA (ODH) EN FASE VAPOR (1), DANDO UNA MEZCLA (5) DE AGUA, DE ACIDO METACRILICO Y DE IMPUREZAS, CUYO ACIDO DE SALIDA NO ESTA CONVERTIDO ; SE CONDENSA LA MEZCLA (EN 6) Y SE REALIZA UNA EXTRACCION LIQUIDO-LIQUIDO (EN 8), PARA SEPARAR EL AGUA (EN 11) DE LOS ACIDOS ORGANICOS (10) ; (EN 21) SE ESTERIFIA ESTOS ACIDOS POR EL METANOL, DANDO UN MMA BRUTO, CON EL ISOBUTIRATO DE METILO COMO IMPUREZA. SE EXTRAE (EN 8) POR UNA FRACCION (9) DEL MMA BRUTO OBTENIDO ; SE ENVIA LA FASE (10) RESULTANTE A UNA ETAPA DE SEPARACION (22), SITUADA ABAJO DE LA ETAPA (21), PARA SEPARAR EL MMA BRUTO (23) (FRACCION DE MMA PRODUCIDO POR LA ESTERIFICACION Y LA UTILIZADA COMO SOLVENTE DE EXTRACCION), Y LOS ACIDOS ORGANICOS (24) (ACIDOS ORGANICOS OBTENIDOS POR EL ODH Y ACIDOS NO ESTERIFICADOS) ; SE PURIFICA (EN 33) LA FRACCION DE MMA BRUTO (32) NO UTILIZADA COMO SOLVENTE DE EXTRACCION, PARA SEPARAR DEL MMA PURO (EN 35) Y DEL ISOBUTIRATO DE METILO (34) RECICLADO EN (1).
ES198989402286T 1988-08-16 1989-08-11 Procedimiento perfeccionado para la fabricacion de metacrilato de metilo a partir del acido isobutirico. Expired - Lifetime ES2034701T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR8810911A FR2635521B1 (fr) 1988-08-16 1988-08-16 Procede perfectionne pour la fabrication de methacrylate de methyle a partir d'acide isobutyrique

Publications (1)

Publication Number Publication Date
ES2034701T3 true ES2034701T3 (es) 1993-04-01

Family

ID=9369335

Family Applications (1)

Application Number Title Priority Date Filing Date
ES198989402286T Expired - Lifetime ES2034701T3 (es) 1988-08-16 1989-08-11 Procedimiento perfeccionado para la fabricacion de metacrilato de metilo a partir del acido isobutirico.

Country Status (11)

Country Link
US (1) US4978776A (es)
EP (1) EP0356315B1 (es)
JP (1) JP2739658B2 (es)
KR (1) KR950006530B1 (es)
AT (1) ATE78022T1 (es)
CA (1) CA1312618C (es)
DE (1) DE68902024T2 (es)
ES (1) ES2034701T3 (es)
FR (1) FR2635521B1 (es)
GR (1) GR3005910T3 (es)
NO (1) NO168578C (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101679187B (zh) * 2007-06-01 2013-06-05 赢创罗姆有限责任公司 用于制备甲基丙烯酸或甲基丙烯酸酯的方法
TW201627267A (zh) * 2014-10-31 2016-08-01 陶氏全球科技公司 用於從氧化性酯化反應中原位水移除的方法使用經耦合的反應器－蒸餾系統
EP4386056A1 (en) * 2022-12-16 2024-06-19 Organik Kimya Sanayi Ve Tic. A.S. Waterborne polymer composition and preparation method thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2541486A (en) * 1948-09-17 1951-02-13 Eastman Kodak Co Acid concentration
FR1393173A (fr) * 1963-05-16 1965-03-19 Distillers Co Yeast Ltd Procédé de production d'acrylate d'éthyle
GB995471A (en) * 1963-05-16 1965-06-16 Distilers Company Ltd Improvements in or relating to the production of ethyl acrylate
US3879446A (en) * 1969-06-05 1975-04-22 Eastman Kodak Co Preparation of unsaturated organic compounds by oxidative dehydrogenation
US3809645A (en) * 1973-04-03 1974-05-07 Mitsubishi Rayon Co Recovering methacrylic acid and methanol
FR2224429A1 (en) * 1973-04-03 1974-10-31 Mitsubishi Rayon Co Recovering methacrylic acid and methanol - by contacting crude products with water, used in methylmethacrylate mfr
US4298755A (en) * 1980-02-25 1981-11-03 Ashland Oil, Inc. Catalytic oxydehydrogenation process
DE3508649A1 (de) * 1985-03-12 1986-09-18 Röhm GmbH, 6100 Darmstadt Heteropolysaeure h(pfeil abwaerts)8(pfeil abwaerts)pmo(pfeil abwaerts)1(pfeil abwaerts)(pfeil abwaerts)0(pfeil abwaerts)vo(pfeil abwaerts)3(pfeil abwaerts)(pfeil abwaerts)9(pfeil abwaerts), deren anhydrid pmo(pfeil abwaerts)1(pfeil abwaerts)(pfeil abwaerts)0(pfeil abwaerts)vo(pfeil abwaerts)3(pfeil abwaerts)(pfeil abwaerts)5(pfeil abwaerts)und ihre verwendung

Also Published As

Publication number Publication date
EP0356315B1 (fr) 1992-07-08
JPH0283354A (ja) 1990-03-23
US4978776A (en) 1990-12-18
FR2635521A1 (fr) 1990-02-23
NO893269L (no) 1990-02-19
GR3005910T3 (es) 1993-06-07
KR950006530B1 (ko) 1995-06-16
NO893269D0 (no) 1989-08-15
ATE78022T1 (de) 1992-07-15
NO168578B (no) 1991-12-02
DE68902024T2 (de) 1993-07-29
KR900003104A (ko) 1990-03-23
JP2739658B2 (ja) 1998-04-15
NO168578C (no) 1992-03-11
EP0356315A1 (fr) 1990-02-28
FR2635521B1 (fr) 1991-02-22
CA1312618C (fr) 1993-01-12
DE68902024D1 (de) 1992-08-13

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