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HRID 547182作成日:2026年10月26日

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

https://huagongshe.com/reaction/547182

反応式

関与物質

役割名称HCID仕込み量
反応物Formic AcidHCID 284—
反応物Sodium HydroxideHCID 14798—
反応物ethyl (3R)-piperidine-3-carboxylateHCID 185582—
反応物Sodium BicarbonateHCID 516892—
溶媒FormaldehydeHCID 712—
生成物ethyl (3R)-1-methylpiperidine-3-carboxylateHCID 73603673%

反応手順

(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE042353E1
出典データセットuspto-grants-2011_05
ORD IDord-c68b3b5ec2e34710853692c235db63a0
出典メモuspto-grants-2011_05