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HRID 1284930생성일: 2026년 10월 26일

Acetonitrile → 4-Fluoro-4'-(N-propyl-carbamyloxy)-alpha-ethyl-benzhydrol

https://huagongshe.com/reaction/1284930

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium CarbonateHCID 11430—
반응물Propyl isocyanateHCID 61033—
반응물4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrolHCID 14727320—
용매EthanolHCID 702—
생성물4-Fluoro-4'-(N-propyl-carbamyloxy)-alpha-ethyl-benzhydrolHCID 14727327—

반응 단계

12.3 g. of 4-fluoro-4'-hydroxy-α-ethyl-benzhydrol, 4.68 g. of n-propyl-isocyanate and 0.7 g. of anhydrous, powdered potassium carbonate in 61 ml. of acetonitrile containing 15 μlit. of a 50% aqueous ethanol solution are refluxed under stirring. When the reaction is complete, the reaction mixture is cooled to room temperature, potassium carbonate is filtered off and acetonitrile is distilled off under reduced pressure. The residue is dissolved in benzene, the benzene solution is shaken with a 5% aqueous sodium hydroxide solution and washed to neutral with water. The organic phase is dried over anhydrous magnesium sulfate, filtered, and benzene is distilled off under reduced pressure. Crystallization of the residue from a mixture of ethyl acetate and n-hexane yields 13.6 g. of the desired compound, melting at 107° to 108° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04564630
출처 데이터셋uspto-grants-1986_01
ORD IDord-4d11fe74511e4c3eb171abfda8490584
출처 메모uspto-grants-1986_01