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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241735Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/241735

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Chlorophenacyl bromideHCID 68303—
EduktO-Ethyl hydrazinecarbothioateHCID 12567113—
LösungsmittelAcetonitrileHCID 6342—
Produkt5-(4-Chlorophenyl)-3,6-dihydro-1,3,4-thiadiazin-2-oneHCID 329473—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653073B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-ac965aab873d4f019cf92ec011495b64
Quellennotizuspto-grants-2014_02