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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412387Generated: November 1, 2026

Phenicarbazide → 1-(beta,beta-Dichloroacryloyl)-1-phenyl-semicarbazide

https://huagongshe.com/reaction/2412387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenicarbazideHCID 61002—
Reactant3,3-Dichloroprop-2-enoyl chlorideHCID 12392131—
SolventAcetonitrileHCID 6342—
Product1-(beta,beta-Dichloroacryloyl)-1-phenyl-semicarbazideHCID 5364671563%

Reaction Steps

To a suspension of 7 g of 1-phenylsemicarbazide in 100 ml of acetonitrile, cooled down to 0°-5° C., were added 7.4 g of β,β-dichloroacryloyl chloride, under stirring. The addition having been completed, the reaction mixture was stirred at 5° C. for 30 minutes and then at room temperature for 1 (one) hour. The solid that separated was collected by decanting and by filtration, then was washed with diethylether, thus obtaining 8 g of 1-(β,β-dichloroacryloyl)-1-phenyl-semicarbazide, in accordance with the elemental analysis and the I.R. and N.M.R. spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04492690
Source datasetuspto-grants-1985_01
ORD IDord-6697b0ec10fa41e087aa349f24102292
Source noteuspto-grants-1985_01