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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896528Generated: October 30, 2026

Triethylamine → 3-(Benzyloxycarbonylaminomethyl)-piperidine-1-carboxylic Acid Tert-butyl Ester

https://huagongshe.com/reaction/896528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant1-Boc-3-(aminomethyl)piperidineHCID 2756483—
SolventDichloromethaneHCID 6344—
Product3-(Benzyloxycarbonylaminomethyl)-piperidine-1-carboxylic Acid Tert-butyl EsterHCID 45158794—

Reaction Steps

A solution of 3-aminomethylpiperidine-1-carboxylic acid tert-butyl ester (2.20 g, 10.3 mmol) in dichloromethane (40 mL) was treated with triethylamine (1.90 mL, 13.3 mmol) and stirred on an ice bath. A solution of benzyl chloroformate (1.90 mL, 13.3 mmol) in dichloromethane (10 mL) was added over 5 minutes. The mixture was stirred at room temperature for 70 hours. It was washed with 0.1 N aqueous hydrochloric acid, dried over sodium sulfate, and concentrated under vacuum to provide a colorless gum (3.58 g, quantitative) which was used without further purification. 1H NMR (300 MHz, CDCl3) δ7.37 (m, 5H), 5.11 (s, 2H), 3.75 (m, 2H), 3.18 (m, 1H), 3.05 (m, 2H), 2.83 (m, 1H), 1.9-1.6 (m, 4H), 1.46 (s, 9H), 1.27 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919356B2
Source datasetuspto-grants-2005_07
ORD IDord-221948ae8b0e4dcc8db64c9b351ccf52
Source noteuspto-grants-2005_07