JPS5798272A - Preparation of 5-(2-cyanoethyl)-2,4-imidazolidinedione - Google Patents

Preparation of 5-(2-cyanoethyl)-2,4-imidazolidinedione

Info

Publication number
JPS5798272A
JPS5798272A JP17514180A JP17514180A JPS5798272A JP S5798272 A JPS5798272 A JP S5798272A JP 17514180 A JP17514180 A JP 17514180A JP 17514180 A JP17514180 A JP 17514180A JP S5798272 A JPS5798272 A JP S5798272A
Authority
JP
Japan
Prior art keywords
reaction
oxobutyronitrile
ammonia
preparation
carbon dioxide
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
JP17514180A
Other languages
Japanese (ja)
Other versions
JPH0114227B2 (en
Inventor
Yasuhiko Inoue
Shigeo Wake
Hidenori Dandan
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP17514180A priority Critical patent/JPS5798272A/en
Publication of JPS5798272A publication Critical patent/JPS5798272A/en
Publication of JPH0114227B2 publication Critical patent/JPH0114227B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE: To prepare the titled substance useful as an intermediate for glutamic acid, etc., in high yield, by reacting 4-oxobutyronitrile, ammonia, carbon dioxide, and hydrocyanic acid, etc. using a specific amount of water as a solvent, in two steps, i.e. at low temperature and high temperaure.
CONSTITUTION: In the preparation of the titled substance by the BUCHERER- BERGS reaction of 4-oxobutyronitrile and/or 2-hydroxypentane dinitrile (the component A), ammonia and/or an ammonium salt, carbon dioxide and/or a carbonate, and hydrocyanic acid and/or its salt, the reaction is carried out using 90W600mol (pref. 90W350mol) of water as a solvent based on 1mol of the component (A), first at room temperature W40°C for 0.5W5hr, and then at 45W110°C for 15minW10hr.
EFFECT: The by-product can be easily and almost completely converted to the objective compound by the acid treatment after the reaction.
COPYRIGHT: (C)1982,JPO&Japio
JP17514180A 1980-12-10 1980-12-10 Preparation of 5-(2-cyanoethyl)-2,4-imidazolidinedione Granted JPS5798272A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17514180A JPS5798272A (en) 1980-12-10 1980-12-10 Preparation of 5-(2-cyanoethyl)-2,4-imidazolidinedione

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17514180A JPS5798272A (en) 1980-12-10 1980-12-10 Preparation of 5-(2-cyanoethyl)-2,4-imidazolidinedione

Publications (2)

Publication Number Publication Date
JPS5798272A true JPS5798272A (en) 1982-06-18
JPH0114227B2 JPH0114227B2 (en) 1989-03-10

Family

ID=15990997

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17514180A Granted JPS5798272A (en) 1980-12-10 1980-12-10 Preparation of 5-(2-cyanoethyl)-2,4-imidazolidinedione

Country Status (1)

Country Link
JP (1) JPS5798272A (en)

Also Published As

Publication number Publication date
JPH0114227B2 (en) 1989-03-10

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