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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1699259생성일: 2026년 10월 25일

Acetaldehyde → 1-Ethyl-4-[1-(phenylmethoxycarbonyl)-4-piperidinyl]piperidine

https://huagongshe.com/reaction/1699259

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물Bromocresol PurpleHCID 8273—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물N-Cbz-4,4'-bipiperidineHCID 10979576—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
용매Methanol--water (1/1)HCID 22242641—
생성물1-Ethyl-4-[1-(phenylmethoxycarbonyl)-4-piperidinyl]piperidineHCID 18321284—

반응 단계

To a solution of 18.14 g (0.061 mol) of 1-(phenylmethoxycarbonyl)-4-(4-piperidinyl)piperidine in 450 ml of a methanol/water mixture (1/1 v/v) were added, with stirring, whilst maintaining a temperature of 15 to 20° C., 10.05 g (0.152 mol) of 95% sodium cyanoborohydride and 50 mg of bromocresol purple. Then a solution of 10.57 g (0.24 mol) of acetaldehyde in 50 ml of methanol and 1N hydrochloric acid were alternately added dropwise so that the colour of the mixture changed continuously from blue to yellow. After all had been added and the reaction had finished the mixture was adjusted to pH 2 with hydrochloric acid and extracted twice with 200 ml of diethylether. The aqueous phase was then made alkaline and extracted thoroughly with dichloromethane. The combined dichloromethane extracts were dried over magnesium sulphate and evaporated down in vacuo. The colourless crystallising residue remaining was purified by column chromatography over silica gel (30-60 μm) using FM1 as eluant. Yield of colourless crystals of melting point 93-96° C.: 7.9 g (39.26 of theory).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06344449B1
출처 데이터셋uspto-grants-2002_02
ORD IDord-392b14df8adc49309bfcd081cf15cacf
출처 메모uspto-grants-2002_02