GB871278A - A process for the production of carboxylic acids - Google Patents

A process for the production of carboxylic acids

Info

Publication number
GB871278A
GB871278A GB42405/59A GB4240559A GB871278A GB 871278 A GB871278 A GB 871278A GB 42405/59 A GB42405/59 A GB 42405/59A GB 4240559 A GB4240559 A GB 4240559A GB 871278 A GB871278 A GB 871278A
Authority
GB
United Kingdom
Prior art keywords
water
catalyst
acids
acid
mono
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
Application number
GB42405/59A
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.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
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 Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Publication of GB871278A publication Critical patent/GB871278A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/10Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
    • C07C51/14Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on a carbon-to-carbon unsaturated bond in organic compounds
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Carboxylic acids are prepared from a monoolefinically unsaturated compound with three or more carbon atoms per molecule, carbon monoxide, and water using an inorganic strong or 'Lewis' acid as catalyst in a process in which liquid catalyst and reactants are continuously supplied to a reaction zone, the amounts of water and mono-olefine being in a molar ratio of more than 1:1, the liquid reaction mixture is kept homogeneous and of constant composition, and the reaction mixture is continuously withdrawn. The reaction zone is stirred or agitated, and a water to olefine ratio of up to 30 : 1, preferably from 2:1 to 6:1 is used, at a temperature of between -10 and 150 DEG C., preferably 40-100 DEG C. and a carbon monoxide pressure of above 20 atoms preferably 50 to 150 atmos. Catalysts include phosphoric, sulphuric acids, hydrated boron trifluoride and its complexes with such acids. Monoolefine compounds specified are propylene and propylene tetramer, butylene-1 and -2, mono- and di-isobutylene, branched and unbranched pentenes, hexenes, heptenes, octenes, nonenes, decenes and higher alkenes, cyclopentene and hexene, and technical mixtures from the thermal vapour phase steam cracking of paraffin wax and an example describes the use of a mixture of 76% alkenes, with 8-10 carbon atoms per molecule, 17% of saturated hydrocarbons with a phosphoric acid-boron trifluoride catalyst. The reactor effluent is separated into two layers by the addition of an organic diluent, the catalyst phase recycled, and the organic phase containing the acid treated by water-washing, conversion to salts e.g. sodium, extraction with gasoline, acidification and fractional distillation. Specifications 743,597 and 798,065 are referred to.
GB42405/59A 1958-12-15 1959-12-14 A process for the production of carboxylic acids Expired GB871278A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL871278X 1958-12-15

Publications (1)

Publication Number Publication Date
GB871278A true GB871278A (en) 1961-06-28

Family

ID=19851213

Family Applications (1)

Application Number Title Priority Date Filing Date
GB42405/59A Expired GB871278A (en) 1958-12-15 1959-12-14 A process for the production of carboxylic acids

Country Status (1)

Country Link
GB (1) GB871278A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001056966A1 (en) * 2000-02-02 2001-08-09 Resolution Research Nederland B.V. MANUFACTURING PROCESS FOR THE PREPARATION OF α-BRANCHED CARBOXYLIC ACIDS HAVING A DECREASED CONTENT OF BETA-BRANCHED ISOMERS
EP1281700A1 (en) * 2001-07-31 2003-02-05 Resolution Research Nederland B.V. Manufacturing process for the preparation of alpha, alpha-branched alkane carboxylic acids providing esters with an improved softness

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001056966A1 (en) * 2000-02-02 2001-08-09 Resolution Research Nederland B.V. MANUFACTURING PROCESS FOR THE PREPARATION OF α-BRANCHED CARBOXYLIC ACIDS HAVING A DECREASED CONTENT OF BETA-BRANCHED ISOMERS
EP1281700A1 (en) * 2001-07-31 2003-02-05 Resolution Research Nederland B.V. Manufacturing process for the preparation of alpha, alpha-branched alkane carboxylic acids providing esters with an improved softness

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