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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1584165생성일: 2026년 10월 26일

Potassium Carbonate → 3-(R)-(1-cyano-1,1-diphenylmethyl)-1-[2-(indan-5-yl)ethyl]piperidine

https://huagongshe.com/reaction/1584165

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-(2-bromoethyl)-2,3-dihydro-1H-indeneHCID 21224080—
반응물3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidineHCID 22853758—
용매AcetonitrileHCID 6342—
생성물3-(R)-(1-cyano-1,1-diphenylmethyl)-1-[2-(indan-5-yl)ethyl]piperidineHCID 22853751—

반응 단계

A mixture containing 3-(R)-(+)-(1-cyano-1,1,-diphenylmethyl)-piperidine (0.28 g), 5-(2-bromoethyl)indane (0.23 g--see Preparation 4), anhydrous potassium carbonate (0.3 g) and acetonitrile (10 ml) was heated under reflux for 5 hours. The mixture was partitioned between dichloromethane (30 ml) and 10% aqueous potassium carbonate (20 ml), the layers separated, and the aqueous layer extracted with dichloromethane (3×20 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a gum which was purified by column chromatography on silica eluting with hexane containing dichloromethane (30% up to 70%) then dichloromethane containing methanol (0% up to 5%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from acetonitrile to give the title compound as colorless rhombs, yield 0.13 g, m.p. 88-91° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05932594
출처 데이터셋uspto-grants-1999_08
ORD IDord-a344f509afcc4e73aee56e91e4dc4112
출처 메모uspto-grants-1999_08