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JPS5788157A - Preparation of aminoiminoacetic acid - Google Patents

Preparation of aminoiminoacetic acid

Info

Publication number
JPS5788157A
JPS5788157A JP55164729A JP16472980A JPS5788157A JP S5788157 A JPS5788157 A JP S5788157A JP 55164729 A JP55164729 A JP 55164729A JP 16472980 A JP16472980 A JP 16472980A JP S5788157 A JPS5788157 A JP S5788157A
Authority
JP
Japan
Prior art keywords
alkyl
aminoiminoacetic
acid
alkoxyiminoacetic
formulai
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
JP55164729A
Other languages
Japanese (ja)
Other versions
JPS619945B2 (en
Inventor
Kiyoshi Fukui
Kiyomi Okimoto
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.)
Ube Corp
Original Assignee
Ube 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 Ube Industries Ltd filed Critical Ube Industries Ltd
Priority to JP55164729A priority Critical patent/JPS5788157A/en
Publication of JPS5788157A publication Critical patent/JPS5788157A/en
Publication of JPS619945B2 publication Critical patent/JPS619945B2/ja
Granted legal-status Critical Current

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

Abstract

PURPOSE: To obtain aminoiminoacetic acid useful as a germicide and insecticide for agricultural and horticultural use in high yield, by reacting an alkoxyiminoacetic ester with a specific amine, and hydrolyzing the reaction product.
CONSTITUTION: An alkoxyiminoacetic ester of formulaI(R1 and R2 are 1W4C alkyl) is reacted with an amine of formula II (R3 is 1W6C alkyl; R4 is 1W6C alkyl or benzyl, R3 and R4 together form a ring through the oxygen atom if necessary when R4 is alkyl). The reaction is carried out in the presence or absence of a solvent, e.g. methanol, at 0W100°C. The resultant reaction product is then hydrolyzed to give the aimed aminoiminoacetic acid. The amount of water used in the hydrolysis is 1W5l based on one mole raw material compound of formulaI, and the hydrolysis is carried out at room temperature for 15W 60min.
COPYRIGHT: (C)1982,JPO&Japio
JP55164729A 1980-11-25 1980-11-25 Preparation of aminoiminoacetic acid Granted JPS5788157A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP55164729A JPS5788157A (en) 1980-11-25 1980-11-25 Preparation of aminoiminoacetic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55164729A JPS5788157A (en) 1980-11-25 1980-11-25 Preparation of aminoiminoacetic acid

Publications (2)

Publication Number Publication Date
JPS5788157A true JPS5788157A (en) 1982-06-01
JPS619945B2 JPS619945B2 (en) 1986-03-27

Family

ID=15798786

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55164729A Granted JPS5788157A (en) 1980-11-25 1980-11-25 Preparation of aminoiminoacetic acid

Country Status (1)

Country Link
JP (1) JPS5788157A (en)

Also Published As

Publication number Publication date
JPS619945B2 (en) 1986-03-27

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