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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2168787생성일: 2026년 10월 25일

Sodium borohydride → tert-Butyl 4-hydroxy-3-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2168787

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물1-(1,1-Dimethylethyl) 3-ethyl 4-oxo-1,3-piperidinedicarboxylateHCID 6420876—
용매MethanolHCID 887—
생성물tert-Butyl 4-hydroxy-3-(hydroxymethyl)piperidine-1-carboxylateHCID 66717856—

반응 단계

To a stirred solution of 4-oxo-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (51.59 mmol, 14 g) in methanol (300 mL) was added sodium borohydride (12 g) in 12 portions over 30 min. The reaction mixture was stirred for additional 30 min, and the volatiles were removed under reduced pressure. To the residue was added saturated ammonium chloride (300 mL). The mixture was extracted with ethyl acetate (300 mL), and the organic layer was dried and concentrated under reduced pressure. The residue was purified on a flash silica gel column eluting with ethyl acetate to provide 4-hydroxy-3-hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09045461B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-c3be25c41d0f4120a740315b5de3f708
출처 메모uspto-grants-2015_06