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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801565Generated: October 30, 2026

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

https://huagongshe.com/reaction/1801565

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 extracted 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 numberUS08349833B2
Source datasetuspto-grants-2013_01
ORD IDord-61598da507cf4a8e9b414b914f5dbfec
Source noteuspto-grants-2013_01