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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013558Generated: November 3, 2026

Benzyl chloroformate → Benzyl 3-acetylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1013558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(Piperidin-3-yl)ethan-1-oneHCID 21909488—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-acetylpiperidine-1-carboxylateHCID 53249939—

Reaction Steps

To a solution of 1-(piperidin-3-yl)ethanone (53, 2.6 g, 20 mmol) in DCM (100 ml) at room temperature was added DIEA (5.2 ml, 30 mmol). A solution of Cbz-Cl (4.4 ml, 30 mmol) in DCM (20 ml) was added dropwise over 2 hrs. The mixture was stirred at room temperature for 17 hrs, washed with water, saturated sodium bicarbonate (aq.), water, 1N HCl (aq.) and brine, dried over anhydrous sodium sulfate. The drying agent was removed by filtration. The filtrate was concentrated under vacuum to give the benzyl 3-acetylpiperidine-1-carboxylate (54) which was used in the next step without further purification. LC-MS for C15H19NO3 calcd: 261; found: 262.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981925B2
Source datasetuspto-grants-2011_07
ORD IDord-56088956e3b349dbb8f2ff9c64bfdaa7
Source noteuspto-grants-2011_07