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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445987Generated: October 29, 2026

Benzyl chloroformate → 1-Boc-4-Cbz-amino-piperidine

https://huagongshe.com/reaction/445987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
SolventDichloromethaneHCID 6344—
Product1-Boc-4-Cbz-amino-piperidineHCID 151430578.5%

Reaction Steps

tert-Butyl 4-aminopiperidine-1-carboxylate (10 g, 49.9 mmol), N,N-diisopropylethylamine (26 ml, 149 mmol), benzyl chloroformate (8.5 ml, 59.5 mmol) and dichloromethane (dehydrated) (300 ml) were mixed under ice-cooling. The resulting mixture was stirred at room temperature for one hour. An aqueous saturated sodium bicarbonate solution was added to the reaction mixture, which was extracted with dichloromethane three times. The organic layer was washed with brine and dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (silica gel, elution solvent: ethyl acetate/heptane) to give the title compound (13.1 g, yield 78.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476301B2
Source datasetuspto-grants-2013_07
ORD IDord-a7fae4ba6124453ca28d8f79c52ffbc0
Source noteuspto-grants-2013_07