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HRID 241735作成日:2026年10月26日

p-Chlorophenacyl bromide → 5-(4-Chlorophenyl)-3,6-dihydro-1,3,4-thiadiazin-2-one

https://huagongshe.com/reaction/241735

反応式

関与物質

役割名称HCID仕込み量
反応物p-Chlorophenacyl bromideHCID 68303—
反応物O-Ethyl hydrazinecarbothioateHCID 12567113—
溶媒AcetonitrileHCID 6342—
生成物5-(4-Chlorophenyl)-3,6-dihydro-1,3,4-thiadiazin-2-oneHCID 329473—

反応手順

A mixture of 2-bromo-1-(4-chloro-phenyl)-ethanone (90.71 mmoles) and hydrazine-carbothioic acid O-ethyl ester (90.71 mmoles) in acetonitrile (84 ml) is stirred at ambient temperature for 3 hours. The solid formed is filtered off, washed with acetonitrile and ethyl ether and then dried in vacuo to yield the title product, which is used directly in the next Step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653073B2
出典データセットuspto-grants-2014_02
ORD IDord-ac965aab873d4f019cf92ec011495b64
出典メモuspto-grants-2014_02