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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44282Generated: October 27, 2026

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

https://huagongshe.com/reaction/44282

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Chlorophenacyl bromideHCID 68303—
ReactantO-Ethyl hydrazinecarbothioateHCID 12567113—
SolventAcetonitrileHCID 6342—
Product5-(4-Chlorophenyl)-3,6-dihydro-1,3,4-thiadiazin-2-oneHCID 329473—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541412B2
Source datasetuspto-grants-2013_09
ORD IDord-1ac677b44aaf48988d0fdf72e6301e2f
Source noteuspto-grants-2013_09