GB782773A - Chlorination process - Google Patents

Chlorination process

Info

Publication number
GB782773A
GB782773A GB2009255A GB2009255A GB782773A GB 782773 A GB782773 A GB 782773A GB 2009255 A GB2009255 A GB 2009255A GB 2009255 A GB2009255 A GB 2009255A GB 782773 A GB782773 A GB 782773A
Authority
GB
United Kingdom
Prior art keywords
chloride
chloroacetyl chloride
examples
chlorine
advantageously
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
GB2009255A
Inventor
Richard Norman Lacey
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.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
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 Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB2009255A priority Critical patent/GB782773A/en
Publication of GB782773A publication Critical patent/GB782773A/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
    • C07C51/58Preparation of carboxylic acid halides

Landscapes

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

Abstract

Chloroacetyl chloride is prepared by interacting chlorine and ketene in the liquid phase in an alkyl acetate. The reaction temperature is preferably below 50 DEG C. and advantageously between 20 DEG and 30 DEG C., and a molar excess of chlorine is preferably employed. The acetate suitably contains less than 8 carbon atoms per molecule and its volume is preferably at least 40 per cent, and advantageously 50 to 70 per cent, of that of the total reaction mixture. In a modification the acetyl chloride formed as a by-product is reacted after separation from the chloroacetyl chloride with an appropriate alkanol to form further quantities of alkyl acetate. The products of the reaction may be separated by fractional distillation, under reduced pressure for the higher boiling products including chloroacetyl chloride. Examples are given, and comparative examples in which carbon tetrachloride, light petroleum, acetyl chloride, chloroacetyl chloride and diisopropyl ether are used as diluents are provided, the yield of dichloroacetyl chloride by-product in these examples being given.
GB2009255A 1955-07-12 1955-07-12 Chlorination process Expired GB782773A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2009255A GB782773A (en) 1955-07-12 1955-07-12 Chlorination process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2009255A GB782773A (en) 1955-07-12 1955-07-12 Chlorination process

Publications (1)

Publication Number Publication Date
GB782773A true GB782773A (en) 1957-09-11

Family

ID=10140243

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2009255A Expired GB782773A (en) 1955-07-12 1955-07-12 Chlorination process

Country Status (1)

Country Link
GB (1) GB782773A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3758571A (en) * 1971-10-26 1973-09-11 Monsanto Co Preparation of monohaloacetyl halides
US4143067A (en) * 1976-12-22 1979-03-06 Lonza, Ltd. Process for the production of chloroacetyl chloride
US4801750A (en) * 1981-03-26 1989-01-31 Lonza Ltd. Process for the produciton of 2-chloroacetoacetic acid amides
CN113087617A (en) * 2021-03-10 2021-07-09 江苏琦衡农化科技有限公司 Preparation method and preparation device of trichloroacetyl chloride

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3758571A (en) * 1971-10-26 1973-09-11 Monsanto Co Preparation of monohaloacetyl halides
US4143067A (en) * 1976-12-22 1979-03-06 Lonza, Ltd. Process for the production of chloroacetyl chloride
US4801750A (en) * 1981-03-26 1989-01-31 Lonza Ltd. Process for the produciton of 2-chloroacetoacetic acid amides
CN113087617A (en) * 2021-03-10 2021-07-09 江苏琦衡农化科技有限公司 Preparation method and preparation device of trichloroacetyl chloride

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