Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301751Generated: October 29, 2026

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

https://huagongshe.com/reaction/2301751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
SolventDichloromethaneHCID 6344—
Product1-Boc-4-Cbz-amino-piperidineHCID 151430596.7%

Reaction Steps

To a solution of 1.2 g (6.0 mmol) 4-amino-1-t-butoxycarbonylpiperidine from Step B in 40 mL of methylene chloride was added 3.15 mL (18 mmol) of DIPEA and 1.03 mL (7.2 mmol) of benzyl chloroformate while cooled in an ice bath. After 0.5 h the reaction was quenched with aqueous sodium carbonate and extracted three times with methylene chloride. The organic layers were each washed with a portion of brine, dried over sodium sulfate, combined and concentrated. The residue was purified by FC eluting with 25% ethyl acetate in hexanes to afford 1.94 g of title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500844B1
Source datasetuspto-grants-2002_12
ORD IDord-40f0d86ad39b49949ecc8ca6e5ed9876
Source noteuspto-grants-2002_12