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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 267193생성일: 2026년 10월 26일

Potassium borohydride → 4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanol

https://huagongshe.com/reaction/267193

반응식

참여 물질

역할이름HCID투입량
반응물Potassium borohydrideHCID 4192641—
반응물Sodium MethoxideHCID 10942334—
반응물4-[4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]piperidino]butyrophenone hydrochlorideHCID 21555731—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanolHCID 21555715—

반응 단계

To a mixture of 4.2 g (0.0083 mole) of 4-[4-[α-(p tert-butylphenyl)-α-hydroxybenzyl]piperidino]butyrophenone hydrochloride and 0.54 g (0.01 mole) of sodium methoxide in 25 ml of methanol is added 2.16 g (0.04 mole) of potassium borohydride. The reaction mixture is stirred overnight, diluted with water and the methanol removed under reduced pressure. The remaining material is extracted with chloroform, washed with water, dried over magnesium sulfate and filtered. The filtrate is concentrated, and the residue is recrystallized from acetone-water to give 4-[α-(p-tert-butylphenyl)-α-hydroxybenzyl]-α-phenyl-1-piperidinebutanol, M.P. 161°-163°C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03941795
출처 데이터셋uspto-grants-1976_03
ORD IDord-31d54994f1804563936e334fbdce7530
출처 메모uspto-grants-1976_03