JPS57209262A - 3-chloro-4-hydroxy-5-cyanophenylacetic acid and its preparation - Google Patents

3-chloro-4-hydroxy-5-cyanophenylacetic acid and its preparation

Info

Publication number
JPS57209262A
JPS57209262A JP9554681A JP9554681A JPS57209262A JP S57209262 A JPS57209262 A JP S57209262A JP 9554681 A JP9554681 A JP 9554681A JP 9554681 A JP9554681 A JP 9554681A JP S57209262 A JPS57209262 A JP S57209262A
Authority
JP
Japan
Prior art keywords
chloro
hydroxy
acid
equivalents
reaction
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
JP9554681A
Other languages
Japanese (ja)
Other versions
JPH0116825B2 (en
Inventor
Mitsuhiro Goi
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.)
Nippon Synthetic Chemical Industry Co Ltd
Original Assignee
Nippon Synthetic Chemical Industry 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 Nippon Synthetic Chemical Industry Co Ltd filed Critical Nippon Synthetic Chemical Industry Co Ltd
Priority to JP9554681A priority Critical patent/JPS57209262A/en
Publication of JPS57209262A publication Critical patent/JPS57209262A/en
Publication of JPH0116825B2 publication Critical patent/JPH0116825B2/ja
Granted legal-status Critical Current

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

Abstract

NEW MATERIAL:A 3-chloro-4-hydroxy-5-cyanophenylacetic acid of the formula (R is H or alkyl).
EXAMPLE: 3-Chloro-4-hydroxy-5-cyanophenylacetic acid.
USE: An intermediate for medicines and organic synthetic intermediate.
PROCESS: 3-Chloro-4-hydroxy-5-aminophenylacetic acid is diazotized and then reacted with a metallic cyanide, e.g. cuprous cyanide, to give the compound of the formula. The diazotation is generally carried out by dissolving the raw material amine in a dilute inorganic acid, and adding sodium nitrite thereto. The necessary theoretical amount of the acid is two equivalents, but usually 2.5W3 equivalents for preventing the formation of a diazoamino compound as a by-product. The sodium nitrite is used in an equivalent amount, and the end point of the reaction is examined by with potassium iodide starch paper. The reaction is usually carried out at 0W15°C.
COPYRIGHT: (C)1982,JPO&Japio
JP9554681A 1981-06-19 1981-06-19 3-chloro-4-hydroxy-5-cyanophenylacetic acid and its preparation Granted JPS57209262A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9554681A JPS57209262A (en) 1981-06-19 1981-06-19 3-chloro-4-hydroxy-5-cyanophenylacetic acid and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9554681A JPS57209262A (en) 1981-06-19 1981-06-19 3-chloro-4-hydroxy-5-cyanophenylacetic acid and its preparation

Publications (2)

Publication Number Publication Date
JPS57209262A true JPS57209262A (en) 1982-12-22
JPH0116825B2 JPH0116825B2 (en) 1989-03-27

Family

ID=14140561

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9554681A Granted JPS57209262A (en) 1981-06-19 1981-06-19 3-chloro-4-hydroxy-5-cyanophenylacetic acid and its preparation

Country Status (1)

Country Link
JP (1) JPS57209262A (en)

Also Published As

Publication number Publication date
JPH0116825B2 (en) 1989-03-27

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