GB654015A - The manufacture of methyl lactate - Google Patents

The manufacture of methyl lactate

Info

Publication number
GB654015A
GB654015A GB2635148A GB2635148A GB654015A GB 654015 A GB654015 A GB 654015A GB 2635148 A GB2635148 A GB 2635148A GB 2635148 A GB2635148 A GB 2635148A GB 654015 A GB654015 A GB 654015A
Authority
GB
United Kingdom
Prior art keywords
lactic acid
methanol
methyl lactate
dehydrated
per cent
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
GB2635148A
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.)
HUGH CAMPBELL HIGHET
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
HUGH CAMPBELL HIGHET
Distillers Co Yeast Ltd
Distillers Co 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 HUGH CAMPBELL HIGHET, Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical HUGH CAMPBELL HIGHET
Priority to GB2635148A priority Critical patent/GB654015A/en
Publication of GB654015A publication Critical patent/GB654015A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/66Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • C07C69/67Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
    • C07C69/675Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids of saturated hydroxy-carboxylic acids
    • C07C69/68Lactic acid esters

Landscapes

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

Abstract

A manufacture of methyl lactate comprises heating lactic acid and/or dehydrated lactic acid and methanol at a temperature between 180 DEG and 235 DEG C. and at a pressure sufficient to keep a major part of the methanol in the liquid phase and maintaining the reaction mixture at said temperature between 30 and 60 minutes. The lactic acid may be anhydrous, dehydrated, i.e. consisting mainly of lactyl and higher polylactyl lactic acids, or contain water, e.g. up to 50 per cent by weight. Acidic esterification catalysts such as boric, phosphoric, toluene sulphonic or sulphuric acids may be present. Entraining liquids such as benzene and toluene present in dehydrated lactic acid are not objectionable. The process may be carried out batchwise, but continuous operation is preferred. In the latter lactic acid and methanol are introduced into a heated reaction zone, most conveniently a long, narrow tube of mild or stainless steel, the rate of flow being adjusted to give a residence time of 30 to 60 minutes. The methyl lactate may be recovered from the reaction mixture by usual methods, e.g. distillation. Methyl lactate is obtained by the rapid fractionation of the products obtained in examples: (1) by passing a mixture of methanol and lactic acid of about 98 per cent concentration through heated mild steel coil under pressure; (2) by passing lactic acid containing 20 per cent by weight of water together with paratoluene sulphonic acid through the same heated coil under pressure.
GB2635148A 1948-10-09 1948-10-09 The manufacture of methyl lactate Expired GB654015A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2635148A GB654015A (en) 1948-10-09 1948-10-09 The manufacture of methyl lactate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2635148A GB654015A (en) 1948-10-09 1948-10-09 The manufacture of methyl lactate

Publications (1)

Publication Number Publication Date
GB654015A true GB654015A (en) 1951-05-30

Family

ID=10242316

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2635148A Expired GB654015A (en) 1948-10-09 1948-10-09 The manufacture of methyl lactate

Country Status (1)

Country Link
GB (1) GB654015A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE957574C (en) * 1954-04-01 1957-02-07 Riedel De Haeen Ag Process for the preparation of oxyarylcarboxylic acid esters

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE957574C (en) * 1954-04-01 1957-02-07 Riedel De Haeen Ag Process for the preparation of oxyarylcarboxylic acid esters

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