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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1176227생성일: 2026년 10월 26일

Benzyl formate → Benzyl 3-hydroxy-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/1176227

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl formateHCID 7708—
반응물Sodium CarbonateHCID 10340—
반응물4-{4-[3-(2-Methoxybenzyloxy)propoxy]phenyl}piperidin-3-olHCID 68503440—
용매Ethyl AcetateHCID 8857—
생성물Benzyl 3-hydroxy-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylateHCID 68499596—

반응 단계

The solution of 3.0 g of 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidin-3-ol in 30 ml of ethyl acetate is cooled to 0° C. with stirring and admixed with 30 ml of saturated aqueous sodium carbonate solution. At 0-5° C., 1.32 ml of benzyl formate are added dropwise. After 10 minutes, the reaction mixture is poured onto water (250 ml) and extracted with ethyl acetate (2×250 ml). The organic phases are washed with brine (1×250 ml), dried over sodium sulphate and concentrated by evaporation. The title compound is obtained as a yellow oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.35 (1:1 EtOAc-heptane); Rt=5.94. m.p. 71-73° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07842688B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-ed19945ce2944ad89c9b8528d6d1a000
출처 메모uspto-grants-2010_11