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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725640Generated: October 31, 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → Tert-butyl 4-[(2-ethoxy-2-oxoethyl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1725640

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductTert-butyl 4-[(2-ethoxy-2-oxoethyl)amino]piperidine-1-carboxylateHCID 1538072483.5%

Reaction Steps

Sodium cyanoborohydride (189 mg, 3.01 mmol) was added to a solution of 1-boc-4-piperidone (500 mg, 2.51 mmol) and glycine ethyl ester hydrochloride (350 mg, 2.51 mmol) in methanol (12.5 mL). After 16 h, the mixture was quenched with saturated ammonium chloride solution, concentrated, and partitioned between dichloromethane and saturated sodium bicarbonate solution. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated. Purification by silica gel chromatography [100% dichloromethane→95% dichloromethane/5% (10% ammonium hydroxide/methanol)] gave the title compound (600 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491713B2
Source datasetuspto-grants-2009_02
ORD IDord-71934f819a8c472dab808ddb4f6eba3f
Source noteuspto-grants-2009_02