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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634264Generated: October 30, 2026

4-Nitrobenzyl chloroformate → HCID 18677664, compound

https://huagongshe.com/reaction/1634264

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-(tert-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 FC 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 numberUS06506777B1
Source datasetuspto-grants-2003_01
ORD IDord-a1ededd305de4a40a13def76090bd285
Source noteuspto-grants-2003_01