戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 345953作成日:2026年10月26日

Thionyl Chloride → 4-Bromo-2-Thiophenecarbonyl Chloride

https://huagongshe.com/reaction/345953

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物4-Bromo-2-thiophenecarboxylic AcidHCID 610409—
生成物4-Bromo-2-Thiophenecarbonyl ChlorideHCID 2795483—

反応手順

According to the procedure of Preparation A, 2.48 g (12.0 mmoles) of 4-bromo-2-thiophenecarboxylic acid (prepared according to Lawesson, S. O., Arkiv. for Kemi. 11:317 (1957)) and 10 ml of thionyl chloride were combined and heated. The reaction gave 2.99 g of 4-bromo-2-thiophenecarbonyl chloride as a dark oil. The acid chloride, 2.11 g (10.0 mmoles) of 5-chloro-2,3-dihydro-2-oxo-1H-indole-1-carboxamide and 3.67 g (30.0 mmoles) of 4-(N,N-dimethylamino)pyridine were reacted in N,N-dimethylformamide to give 4.03 g of a crude orange solid. Recrystallization gave 2.67 g (6.68 mmoles, 66.8% yield) of title compound as a yellow crystalline solid, m.p. 217°-219° C. (dec.) (2-butanone).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05059693
出典データセットuspto-grants-1991_10
ORD IDord-3d4a37c19f174497bf81c42705289de9
出典メモuspto-grants-1991_10