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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547182생성일: 2026년 10월 25일

Formic Acid → ethyl (3R)-1-methylpiperidine-3-carboxylate

https://huagongshe.com/reaction/547182

반응식

참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물Sodium HydroxideHCID 14798—
반응물ethyl (3R)-piperidine-3-carboxylateHCID 185582—
반응물Sodium BicarbonateHCID 516892—
용매FormaldehydeHCID 712—
생성물ethyl (3R)-1-methylpiperidine-3-carboxylateHCID 73603673%

반응 단계

(R)-Ethyl nipecotate (5.7 g 365 mmol), (prepared by resolution of ethyl nipecotate by treatment with L(+)-tartaric acid as described in J. Org. Chem. 1991, (56), 1168), was dissolved in 38.5% aqueous formaldehyde solution (45 ml) and formic acid (90 ml) and the mixture heated at reflux for 18 hours. The mixture was allowed to cool and added dropwise to cooled saturated aqueous sodium hydrogen carbonate solution. The mixture was adjusted to pH12 by addition of sodium hydroxide and the mixture was extracted with methylene chloride. The organic extract was washed with brine, dried (MgSO4) and the solvent removed by evaporation to give (R)-ethyl 1-methylpiperidine-3-carboxylate (4.51 g, 73%) as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE042353E1
출처 데이터셋uspto-grants-2011_05
ORD IDord-c68b3b5ec2e34710853692c235db63a0
출처 메모uspto-grants-2011_05