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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301756Generated: October 31, 2026

4-Nitrobenzyl chloroformate → HCID 18677664, compound

https://huagongshe.com/reaction/2301756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl chloroformateHCID 78205—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 4-[(prop-2-en-1-yl)amino]piperidine-1-carboxylateHCID 18677683—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 18677664HCID 1867766482.1%

Reaction Steps

A portion of the crude 4-(allylamino)-1-(t-butoxycarbonyl)piperidine (400 mg, 1.66 mmol) was dissolved in 10 mL of dichloromethane and treated with N,N-diisopropylethylamine (0.700 mL, 519 mg, 4.0 mmol) and 4-nitrobenzyl chloroformate (392 mg, 1.82 mmol). After stirring 3 h at rt, the mixture was diluted with 30 mL of ethyl acetate and washed with 15 mL each of 2 N aqueous HCl, saturated aqueous sodium bicarbonate, and brine. The organic layer was dried over sodium sulfate, and evaporated. The residue was purified by flash column chromatography on silica gel, eluting with 30% ethyl acetate in hexane, to give 572 mg of the title compound as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500844B1
Source datasetuspto-grants-2002_12
ORD IDord-9b001e08610a49fc9a21ec07b293eaf9
Source noteuspto-grants-2002_12