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JPS56150026A - Preparation of methyl chloride - Google Patents

Preparation of methyl chloride

Info

Publication number
JPS56150026A
JPS56150026A JP5269480A JP5269480A JPS56150026A JP S56150026 A JPS56150026 A JP S56150026A JP 5269480 A JP5269480 A JP 5269480A JP 5269480 A JP5269480 A JP 5269480A JP S56150026 A JPS56150026 A JP S56150026A
Authority
JP
Japan
Prior art keywords
chloride
catalyst
methyl
methyl chloride
quaternary ammonium
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.)
Pending
Application number
JP5269480A
Other languages
Japanese (ja)
Inventor
Kiichi Habata
Kesaji Ichikawa
Mutsuo Shimizu
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.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Chemical 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 Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP5269480A priority Critical patent/JPS56150026A/en
Publication of JPS56150026A publication Critical patent/JPS56150026A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PURPOSE: To obtain methyl chloride in high yield and purity, at lower temperatures in a high reaction rate and a longer catalyst life in the reaction of methyl alcohol with hydrogen chloride, by using a quaternary ammonium halide salt as a catalyst.
CONSTITUTION: Methyl alcohol in an amount of about 10W30% excess, is reacted with hydrogen chloride in the presence of a quaternary ammonium halide salt, preferably a quaternary salt of pyridine, more preferably N-methyl pyridinium chloride, at about 100W200°C, preferably 130W150°C, to give methyl chloride at low temperatures at a sufficiently high reaction rate. This method has advantages as follows: very little dimethyl ether is formed as a by-product and the purification after the readily achieved due to the difficult entrainment of the catalyst by the methyl chloride. The catalyst has a very long life, and the reaction volume for a given production may be smaller than the conventional one.
COPYRIGHT: (C)1981,JPO&Japio
JP5269480A 1980-04-21 1980-04-21 Preparation of methyl chloride Pending JPS56150026A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5269480A JPS56150026A (en) 1980-04-21 1980-04-21 Preparation of methyl chloride

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5269480A JPS56150026A (en) 1980-04-21 1980-04-21 Preparation of methyl chloride

Publications (1)

Publication Number Publication Date
JPS56150026A true JPS56150026A (en) 1981-11-20

Family

ID=12921986

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5269480A Pending JPS56150026A (en) 1980-04-21 1980-04-21 Preparation of methyl chloride

Country Status (1)

Country Link
JP (1) JPS56150026A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6197249A (en) * 1984-10-18 1986-05-15 ザ ブリテイツシユ ピトローリアム コンパニー ピー.エル.シー Manufacture of alkoxyhalide
DE102005008547A1 (en) * 2005-02-23 2006-08-31 Degussa Ag Process for the preparation of alkyl chlorides
EP1663921B2 (en) 2003-09-08 2010-08-25 Basf Se Method for producing haloalkanes from alcohols
JP2012031129A (en) * 2010-06-29 2012-02-16 Kuraray Co Ltd Method for producing primary alkyl halide
US8859830B2 (en) 2009-03-05 2014-10-14 Dow Global Technologies Inc. Methods and assemblies for liquid-phase reactions

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6197249A (en) * 1984-10-18 1986-05-15 ザ ブリテイツシユ ピトローリアム コンパニー ピー.エル.シー Manufacture of alkoxyhalide
EP1663921B2 (en) 2003-09-08 2010-08-25 Basf Se Method for producing haloalkanes from alcohols
DE102005008547A1 (en) * 2005-02-23 2006-08-31 Degussa Ag Process for the preparation of alkyl chlorides
JP2006232830A (en) * 2005-02-23 2006-09-07 Degussa Ag Method for producing alkyl chloride
DE102005008547B4 (en) * 2005-02-23 2007-10-04 Degussa Gmbh Process for the preparation of alkyl chlorides
US8859830B2 (en) 2009-03-05 2014-10-14 Dow Global Technologies Inc. Methods and assemblies for liquid-phase reactions
JP2012031129A (en) * 2010-06-29 2012-02-16 Kuraray Co Ltd Method for producing primary alkyl halide

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