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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387503Generated: November 1, 2026

Benzyl chloroformate → Benzyl 3-acetylpiperidine-1-carboxylate

https://huagongshe.com/reaction/387503

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 numberUS08372991B2
Source datasetuspto-grants-2013_02
ORD IDord-b00315dca625415fbf7f005e78fa0e42
Source noteuspto-grants-2013_02