Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526482Generated: November 2, 2026

Ethyl Acetate → tert-Butyl 4-(3-ethoxy-3-oxopropanoyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1526482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylateHCID 2758812—
Producttert-Butyl 4-(3-ethoxy-3-oxopropanoyl)piperidine-1-carboxylateHCID 661886852.1%

Reaction Steps

To a mixture of ethyl N-Boc-piperidine-4-carboxylate (0.5 mol) and ethyl acetate (3 mol) t-BuOK (1.5 mol) was added in some portions at 0 C. The mixture was stirred at room temperature for 3 h (monitored by TLC), concentrated up to a half of volume, diluted with water (200 mL) and extacted with ether. Organic layer was dried over sodium sulfate and evaporated in vacuo. Purification by column chromatography (silica gel, ethyl acetate/hexane) afforded 4-(2-ethoxycarbonyl-acetyl)-piperidine-1-carboxylic acid tert-butyl ester (78 g, 52%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085585B2
Source datasetuspto-grants-2015_07
ORD IDord-fd8778db6bfe4a9c87458c6dd0de9809
Source noteuspto-grants-2015_07