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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397677Generated: October 31, 2026

Benzyl chloroformate → Benzyl 3-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/397677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantPiperidin-3-ylmethanolHCID 107308—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2776577—

Reaction Steps

Benzyl chloroformate (7.88 ml) was added over ten minutes to an ice-cold solution of 3-hydroxymethyl piperidine (5.76 g) and ethyldiisopropylamine (9.58 ml) in dichloromethane (300 ml). The reaction mixture was allowed to warm to room temperature and stirred for 1 hr. The reaction was then diluted with dichloromethane (500 ml), washed with 1N aqueous hydrochloric acid (200 ml), dried over magnesium sulphate, and evaporated to afford benzyl 3-(hydroxymethyl)-1-piperidinecarboxylate as an oil (12.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610707B1
Source datasetuspto-grants-2003_08
ORD IDord-7f0a59083c3b4b7b8eceb5ee96b4ae57
Source noteuspto-grants-2003_08