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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21397생성일: 2026년 10월 24일

Phenethyl bromide → 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)-1-phenethylpiperidine

https://huagongshe.com/ko/reaction/21397

반응식

참여 물질

역할이름HCID투입량
반응물Phenethyl bromideHCID 7666—
반응물Potassium CarbonateHCID 11430—
반응물3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)piperidineHCID 13633748—
용매AcetonitrileHCID 6342—
생성물3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)-1-phenethylpiperidineHCID 21224093—

반응 단계

A mixture containing 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)piperidine (0.3 g), phenethyl bromide (0.2 g), anhydrous potassium carbonate (0.3 g) and acetonitrile (10 ml) was heated under reflux for 7 hours. The mixture was partitioned between dichloromethane (30 ml) and 10% aqueous sodium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (2×30 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a colourless solid which was recrystallised from aqueous ethanol to give the title compound, yield, 0.17 g, m.p. 175°-1780° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05422358
출처 데이터셋uspto-grants-1995_06
ORD IDord-978206fb8dd144ab90f2e261895a7ce5
출처 메모uspto-grants-1995_06