GB343947A - Improvements in or relating to the production of organic compounds containing oxygen - Google Patents

Improvements in or relating to the production of organic compounds containing oxygen

Info

Publication number
GB343947A
GB343947A GB2564729A GB2564729A GB343947A GB 343947 A GB343947 A GB 343947A GB 2564729 A GB2564729 A GB 2564729A GB 2564729 A GB2564729 A GB 2564729A GB 343947 A GB343947 A GB 343947A
Authority
GB
United Kingdom
Prior art keywords
carbon monoxide
methyl
acetate
methyl alcohol
compounds
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
GB2564729A
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.)
Acordis UK Ltd
Original Assignee
British Celanese Ltd
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 British Celanese Ltd filed Critical British Celanese Ltd
Priority to GB2564729A priority Critical patent/GB343947A/en
Publication of GB343947A publication Critical patent/GB343947A/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
    • C07C51/12Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on an oxygen-containing group in organic compounds, e.g. alcohols
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/36Preparation of carboxylic acid esters by reaction with carbon monoxide or formates

Landscapes

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

Abstract

Acetic acid; methyl acetate.-In the production of oxygenated organic compounds, particularly acetic acid and other carboxylic acids and esters thereof, by the action of carbon monoxide on alcohols either in the free or combined state in the presence of inorganic acid catalysts of the type defined in Specification 283,989, [Class 2 (iii), Dyes &c.], promoters comprising vanadium, chromium, manganese, iron, nickel, cobalt, or compounds of these metals, or mixtures thereof with one another or with copper or copper compounds are incorporated in the catalysts. The process is particularly applicable to the production of acetic acid and methyl acetate by the action of carbon monoxide on methyl alcohol or compounds capable of decomposing under the conditions of the reaction with the separation of a methoxy group or methyl alcohol. Such compounds include dimethyl ether or methyl esters such as methyl formate or acetate. When methyl formate is employed carbon monoxide is formed by its decomposition, and in this case the addition of further carbon monoxide, although preferable, may be dispensed with. The proportion of methyl acetate in the product depends on the relative proportions of methyl alcohol, carbon monoxide, and water vapour present in the starting materials. The reaction is preferably carried out at temperatures between 250 DEG and 400 DEG C., and pressure up to 300 atmospheres or more may be employed. Inert gases may be present. The main catalyst may consist of any of the phosphoric acids or a mixture thereof, acid phosphates, or aromatic sulphonic acids. The phosphoric acid may be employed in the liquid form or on an inert solid carrier. The promoter is preferably a compound of iron or manganese, for example, the hydroxide, acetate, or formate of either metal. The apparatus in contact with phosphoric acids may be lined with gold, platinum, or graphite, or made of or lined with copper. According to an example a vapour mixture of methyl alcohol, water, and carbon monoxide obtained by passing carbon monoxide through liquid methyl alcohol at 50-56 DEG C. and afterwards through water at 80 DEG C. is passed at 120-160 atmospheres pressure over a catalyst consisting of pyrophosphoric acid with 0,5-1,0 per cent of iron or manganese formate maintained at 290-315 DEG C. in a gold-lined reaction vessel. The products are separated by condensation, the condensate containing methyl acetate and acetic acid, and the uncondensed gases are returned to the reaction. Hydrocarbon and other undesired products may be removed from the circulating gases by means of absorbents such as active carbon, absorbent charcoal, or silica gel. Specification 317,867, [Class 2 (iii), Dyes &c.], also is referred to.
GB2564729A 1929-08-22 1929-08-22 Improvements in or relating to the production of organic compounds containing oxygen Expired GB343947A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2564729A GB343947A (en) 1929-08-22 1929-08-22 Improvements in or relating to the production of organic compounds containing oxygen

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2564729A GB343947A (en) 1929-08-22 1929-08-22 Improvements in or relating to the production of organic compounds containing oxygen

Publications (1)

Publication Number Publication Date
GB343947A true GB343947A (en) 1931-02-23

Family

ID=10231055

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2564729A Expired GB343947A (en) 1929-08-22 1929-08-22 Improvements in or relating to the production of organic compounds containing oxygen

Country Status (1)

Country Link
GB (1) GB343947A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009117055A1 (en) * 2008-03-17 2009-09-24 Lyondell Chemical Technology, L.P. Removing hydrocarbon impurities from acetic acid production process
WO2010117400A1 (en) * 2009-03-30 2010-10-14 Lyondell Chemical Technology, L.P. Removing hydrocarbon impurities from acetic acid production intermediate

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009117055A1 (en) * 2008-03-17 2009-09-24 Lyondell Chemical Technology, L.P. Removing hydrocarbon impurities from acetic acid production process
WO2010117400A1 (en) * 2009-03-30 2010-10-14 Lyondell Chemical Technology, L.P. Removing hydrocarbon impurities from acetic acid production intermediate
US8586789B2 (en) 2009-03-30 2013-11-19 Lyondell Chemical Technology, L.P. Removing hydrocarbon impurities from acetic acid production intermediate
US8912358B2 (en) 2009-03-30 2014-12-16 Lyondellbasell Acetyls, Llc Removing hydrocarbon impurities from acetic acid production intermediate

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