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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613683Generated: October 25, 2026

4-Chlorobutyrophenone → 2-(4-Chloro-1-phenyl-butylidene)-N-phenyl-hydrazinecarbothioamide

https://huagongshe.com/reaction/613683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobutyrophenoneHCID 253533—
ReactantHydrazinecarbothioamide, N-phenyl-HCID 730679—
SolventEthanolHCID 702—
Product2-(4-Chloro-1-phenyl-butylidene)-N-phenyl-hydrazinecarbothioamideHCID 5374726062.6%

Reaction Steps

A mixture of 4-chlorobutyrophenone (6.7 mL, 42 mmol) and 4-phenyl-3-thiosemicarbazide (7.0 g, 42 mmol) in 500 mL of ethanol was warmed under a nitrogen atmosphere to dissolve all the solids and then the reaction stirred at room temperature for four days. The solid formed was collected by filtration and dried under reduced pressure to give 8.73 g of a white solid. Recrystallization of the solid from ethanol gave 7.99 g (57%) of the title compound as a white solid, mp 107-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008362
Source datasetuspto-grants-1999_12
ORD IDord-a4ace6d1b5ed443c8dd624f2fd2543b9
Source noteuspto-grants-1999_12