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HRID 374350作成日:2026年10月26日

2-Fluoroethyl bromide → 2-(2-Fluoroethylthio)-phenylsulfonamide

https://huagongshe.com/reaction/374350

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluoroethyl bromideHCID 12982—
反応物2-Mercaptophenylsulfonamide triethylamine saltHCID 19809753—
溶媒TetrahydrofuranHCID 8028—
生成物2-(2-Fluoroethylthio)-phenylsulfonamideHCID 19809754571.9%

反応条件

温度0 °C

反応手順

A mixture of 29 g of the 2-mercaptophenylsulfonamide triethylamine salt obtained in accordance with Example H6 and 2 g of 2-bromo-1-fluoroethane in 130 ml of tetrahydrofuran is stirred for 6 hours at a temperature of +40° C. to +45° C. The reaction mixture is then cooled to 0° C. and filtered. The filtrate is evaporated and the resulting residue is crystallized from methylene dichloride to give 21.2 g (90.2% of theory) of 2-(2-fluoroethylthio)-phenylsulfonamide having a melting point of +84° to +85° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05166430
出典データセットuspto-grants-1992_11
ORD IDord-1fb3128e46c04bed8f76a416cf3704e2
出典メモuspto-grants-1992_11