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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857609Generated: November 2, 2026

(S)-tert-Butyl 2-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate → (S)-1-N-Boc-piperidine-2-ethanol

https://huagongshe.com/reaction/1857609

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-Butyl 2-(2-methoxy-2-oxoethyl)piperidine-1-carboxylateHCID 10264438—
ReactantAluminium lithium hydrideHCID 21226445—
Product(S)-1-N-Boc-piperidine-2-ethanolHCID 151424394.6%

Reaction Steps

To a slurry of lithium aluminum hydride (580 mg in 65 mL dry diethyl ether) at 0° C. was added dropwise a solution of (S)-2-(methoxycarbonylmethyl)piperidine-1-carboxylic acid tert-butyl ester (5.47 g in 40 mL dry diethyl ether) over a period of 30 minutes. The reaction was allowed to continue at 0° C. for an additional hour, at which time it was quenched by the careful addition of 0.58 mL water followed by 0.58 mL 2N sodium hydroxide and 1.8 mL water. The resulting suspension was stirred vigorously for 30 minutes then filtered through diatomaceous earth. The filtrate was concentrated in vacuo and the residue purified by flash chromatography on silica gel (hexane:ethyl acetate, 6:4) to give the title compound (4.61 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147088
Source datasetuspto-grants-2000_11
ORD IDord-10feda1f01b34afcbe926e1e7e71fdd4
Source noteuspto-grants-2000_11