JPS6468357A - Production of chloro-2-pyridinol - Google Patents

Production of chloro-2-pyridinol

Info

Publication number
JPS6468357A
JPS6468357A JP22533687A JP22533687A JPS6468357A JP S6468357 A JPS6468357 A JP S6468357A JP 22533687 A JP22533687 A JP 22533687A JP 22533687 A JP22533687 A JP 22533687A JP S6468357 A JPS6468357 A JP S6468357A
Authority
JP
Japan
Prior art keywords
alkali
solution
acid
active carbon
amount
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.)
Granted
Application number
JP22533687A
Other languages
Japanese (ja)
Other versions
JPH0822852B2 (en
Inventor
Noboru Kamei
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.)
Daicel Corp
Original Assignee
Daicel Chemical Industries 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 Daicel Chemical Industries Ltd filed Critical Daicel Chemical Industries Ltd
Priority to JP22533687A priority Critical patent/JPH0822852B2/en
Publication of JPS6468357A publication Critical patent/JPS6468357A/en
Publication of JPH0822852B2 publication Critical patent/JPH0822852B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Pyridine Compounds (AREA)

Abstract

PURPOSE:To improve purity without coloring in obtaining the titled compound useful as an intermediate for insecticides by heating and hydrolyzing chloropyridine in an alkali aqueous solution and adding an acid, adding the acid to adjust pH to a specific value, treating with active carbon and readjusting pH to a given value. CONSTITUTION:Chloropyridine shown by the formula is heated in an aqueous solution of an alkali such as potassium hydroxide and hydrolyzed. Then the hydrolyzed solution is adjusted to pH <7 with an acid. Then the solution is treated with active carbon (the amount of the active carbon added is preferably at least 0.05wt.% based on the amount of the reaction solution), successively readjusted to pH >=7, preferably pH >=8 with an alkali and filtered while being hot to give the aimed compound. The hot filtration is carried out under normal pressure at >=75 deg.C, preferably >=85 deg.C. Dissolved state of the reaction product is required in the hot filtration so that amount of water is selected depending upon the alkali used. The aimed compound is precipitated at pH 2-4 while maintaining the reaction solution at >=80 deg.C after the hot filtration.
JP22533687A 1987-09-10 1987-09-10 Method for producing chloro-2-pyridinol Expired - Lifetime JPH0822852B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22533687A JPH0822852B2 (en) 1987-09-10 1987-09-10 Method for producing chloro-2-pyridinol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22533687A JPH0822852B2 (en) 1987-09-10 1987-09-10 Method for producing chloro-2-pyridinol

Publications (2)

Publication Number Publication Date
JPS6468357A true JPS6468357A (en) 1989-03-14
JPH0822852B2 JPH0822852B2 (en) 1996-03-06

Family

ID=16827752

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22533687A Expired - Lifetime JPH0822852B2 (en) 1987-09-10 1987-09-10 Method for producing chloro-2-pyridinol

Country Status (1)

Country Link
JP (1) JPH0822852B2 (en)

Also Published As

Publication number Publication date
JPH0822852B2 (en) 1996-03-06

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