Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364597Generated: October 30, 2026

Benzyl chloroformate → 1-N-Boc-4-(N-cbz-aminomethyl)piperidine

https://huagongshe.com/reaction/2364597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
SolventDichloromethaneHCID 6344—
Product1-N-Boc-4-(N-cbz-aminomethyl)piperidineHCID 11792026—

Reaction Steps

tert-Butyl 4-(aminomethyl)piperidine-1-carboxylate (0.611 g, 2.851 mmol) and diisopropylethylamine (0.479 g, 3.706 mmol) were dissolved in 30 mls of dry dichloromethane. To this mixture was added benzyl chloroformate (0.552 g, 3.136 mmol) and the mixture was stirred at room temperature for 2 hours. The mixture was then diluted with 50 mls of dichloromethane, washed once with 1N aqueous HCl, one with saturated sodium bicarbonate solution, dried over sodium sulfate and concentrated under reduced pressure to 950 mgs (96%) of the title compound and used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691809B2
Source datasetuspto-grants-2014_04
ORD IDord-0a7e9376de244e2eb290a0b1a278c07d
Source noteuspto-grants-2014_04