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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447031Generated: October 26, 2026

Benzoyl chloride → (alpha-phenyl trifluoroethyl) N'benzoylthio Urea

https://huagongshe.com/reaction/1447031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium thiocyanateHCID 15666—
Reactantalpha-(Trifluoromethyl)benzenemethanamineHCID 89166—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(alpha-phenyl trifluoroethyl) N'benzoylthio UreaHCID 54116461—

Reaction Steps

8.2 g ammonium thiocyanate are dissolved in 54 ml water and the resulting solution is cooled to about 0°. The temperature is kept at this temperature during the addition of a solution of 11.5 ml benzoyl chloride in 10.5 ml acetone thereto. The temperature of the reaction mixture is allowed to revert to about 30° then the mixture is heated to reflux for 10 mn. A solution of α-phenyl trifluoroethylamine in 110 ml. acetone is thereafter added portionwise for 1 hour while heating the mixture at reflux. The heating is maintained for a further period of 11/2 hour then let to revert to ambient temperature. The solvent is distilled off. The dry residue is taken up in 250 ml water. The aqueous solution is extracted 3 times with 200 ml ether. The organic phases are united, washed with water until the washings are free of chlorine ions, filtered and dried on sodium sulphate. The solvent is evaporated off, under reduced pressure and 34.1 g of raw product are recovered. The compound is purified by recrystallizing it from hexane. The pure N-(α-phenyl trifluoroethyl) N'-benzoyl thio Urea melts at 55°-60°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04315019
Source datasetuspto-grants-1982_02
ORD IDord-236c0afc9f374554a443b4987d77010e
Source noteuspto-grants-1982_02