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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509201Generated: October 25, 2026

Benzyl chloroformate → Benzyl 4-benzoylpiperidine-1-carboxylate

https://huagongshe.com/reaction/509201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Benzoylpiperidine hydrochlorideHCID 2724437—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 4-benzoylpiperidine-1-carboxylateHCID 57779495—

Reaction Steps

To a stirring suspension of phenyl(piperidin-4-yl)methanone hydrochloride 86 (1.97 g, 8.73 mmol) and potassium carbonate (3.62 g, 26.2 mmol) in THF (40 mL) at 0° C. was added benzyl chloroformate (1.433 mL, 10.04 mmol) and the reaction mixture was allowed to slowly warm to room temperature and stirred for 2 h. The mixture was diluted with ethyl acetate, washed with brine, water, dried over Na2SO4, filtered and concentrated to afford compound 87 quantitative yield. LRMS (ESI): (calc) 323.39 (found) 324.31 (MH)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096565B2
Source datasetuspto-grants-2015_08
ORD IDord-b2d89e74c61944c2a87bd85c7ce2a969
Source noteuspto-grants-2015_08