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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1447036생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1447036

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물Ammonium thiocyanateHCID 15666—
반응물alpha-(Trifluoromethyl)benzenemethanamineHCID 89166—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물(alpha-phenyl trifluoroethyl) N'benzoylthio UreaHCID 54116461—

반응 단계

8.2 g ammonium thiocyanate are dissolved in 54 ml water and the resulting solution is cooled to about 0°. The temperature is kept to 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 let 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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04315020
출처 데이터셋uspto-grants-1982_02
ORD IDord-3073c733e12e48a199edf28d1b43f9a8
출처 메모uspto-grants-1982_02