JPS56100780A - Thiophene compound and its preparation - Google Patents

Thiophene compound and its preparation

Info

Publication number
JPS56100780A
JPS56100780A JP357180A JP357180A JPS56100780A JP S56100780 A JPS56100780 A JP S56100780A JP 357180 A JP357180 A JP 357180A JP 357180 A JP357180 A JP 357180A JP S56100780 A JPS56100780 A JP S56100780A
Authority
JP
Japan
Prior art keywords
compound
formula
preparation
effected
added
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
JP357180A
Other languages
Japanese (ja)
Inventor
Shoji Tada
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 Kayaku Co Ltd
Original Assignee
Nippon Kayaku 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 Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd
Priority to JP357180A priority Critical patent/JPS56100780A/en
Publication of JPS56100780A publication Critical patent/JPS56100780A/en
Pending legal-status Critical Current

Links

Abstract

NEW MATERIAL:Compounds of formula I (X is H, lower alkyl, carbo-lower- alkoxymethyl).
EXAMPLE: 2-Amino-3-nitrothiophene.
USE: A starting material of dyes and agricultural chemicals.
PREPARATION: Nitroacetonitrile and a compound of SHCH2COX (e.g., α-mercaptoacetaldehyde) are added to a mixed solvent composed of ethanol and water and the condensation reaction is effected by dropping a basic substance such as triethylamine to obtain a thiophene compound of formula I. Further, the compound is dissolved in pyridine and acetyl chloride or the like is added thereto to effect the acylation of the amino group. Then, the nitration is effected with a mixed acid of nitric and sulfuric acids. Finally, the acyl group is hydrolyzed to give the compound of formula II, too.
COPYRIGHT: (C)1981,JPO&Japio
JP357180A 1980-01-18 1980-01-18 Thiophene compound and its preparation Pending JPS56100780A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP357180A JPS56100780A (en) 1980-01-18 1980-01-18 Thiophene compound and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP357180A JPS56100780A (en) 1980-01-18 1980-01-18 Thiophene compound and its preparation

Publications (1)

Publication Number Publication Date
JPS56100780A true JPS56100780A (en) 1981-08-12

Family

ID=11561124

Family Applications (1)

Application Number Title Priority Date Filing Date
JP357180A Pending JPS56100780A (en) 1980-01-18 1980-01-18 Thiophene compound and its preparation

Country Status (1)

Country Link
JP (1) JPS56100780A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115368339A (en) * 2022-09-05 2022-11-22 浙江迪邦化工有限公司 High-yield continuous synthesis method of 2-acetamido-3, 5-dinitrothiophene

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115368339A (en) * 2022-09-05 2022-11-22 浙江迪邦化工有限公司 High-yield continuous synthesis method of 2-acetamido-3, 5-dinitrothiophene
CN115368339B (en) * 2022-09-05 2024-04-05 浙江迪邦化工有限公司 High-yield continuous synthesis method of 2-acetamido-3, 5-dinitrothiophene

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