JPS6452732A - Production of 2-chloro-1-propanol - Google Patents

Production of 2-chloro-1-propanol

Info

Publication number
JPS6452732A
JPS6452732A JP20827087A JP20827087A JPS6452732A JP S6452732 A JPS6452732 A JP S6452732A JP 20827087 A JP20827087 A JP 20827087A JP 20827087 A JP20827087 A JP 20827087A JP S6452732 A JPS6452732 A JP S6452732A
Authority
JP
Japan
Prior art keywords
compound
soluble
chloropropionic
aldehyde
liquid phase
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
JP20827087A
Other languages
Japanese (ja)
Inventor
Kenji Fujiwara
Hiroshi Ono
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP20827087A priority Critical patent/JPS6452732A/en
Publication of JPS6452732A publication Critical patent/JPS6452732A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To efficiently obtain the titled substance useful as an intermediate of various kind of industrial chemicals in high purity, by hydrogenating 2- chloropropionic aldehyde in the presence of a soluble Ru compound, soluble Rh compound or soluble Ir compound in a liquid phase. CONSTITUTION:2-Chloropropionic aldehyde is hydrogenated in the presence of 0.1-10wt.% soluble Ru compound, soluble Rh compound or soluble Ir compound at 40-90 deg.C, 5-100kg/cm<2> hydrogen pressure and liquid phase to provide the titled substance. As the above-mentioned catalyst, oxide, mineral acid salt, organic acid salt, complex compound, etc., of Ru, Rh or Ir is used and e.g. dichlorotris(triphenylphosphine)ruthenium(II) is given. The reaction is carried out preferably in a solvent such as hexane, benzene, cyclohexane or dichloromethane in a raw material concentration of 5-15wt.%.
JP20827087A 1987-08-24 1987-08-24 Production of 2-chloro-1-propanol Pending JPS6452732A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20827087A JPS6452732A (en) 1987-08-24 1987-08-24 Production of 2-chloro-1-propanol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20827087A JPS6452732A (en) 1987-08-24 1987-08-24 Production of 2-chloro-1-propanol

Publications (1)

Publication Number Publication Date
JPS6452732A true JPS6452732A (en) 1989-02-28

Family

ID=16553462

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20827087A Pending JPS6452732A (en) 1987-08-24 1987-08-24 Production of 2-chloro-1-propanol

Country Status (1)

Country Link
JP (1) JPS6452732A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5744655A (en) * 1996-06-19 1998-04-28 The Dow Chemical Company Process to make 2,3-dihalopropanols

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5744655A (en) * 1996-06-19 1998-04-28 The Dow Chemical Company Process to make 2,3-dihalopropanols

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