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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747721Generated: October 27, 2026

Triethylamine → Benzyl 4-Hydroxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/747721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantPiperidin-4-olHCID 79341—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—

Reaction Steps

25.0 g (247 mmol) of 4-hydroxypiperidine was dissolved in 800 ml of dichloromethane. 38 ml (266 mmol) of benzyloxycarbonyl chloride and 75 ml (538 mmol) of triethylamine were added to the solution at 0° C., and they were stirred at room temperature for 15 hours. After the treatment with dichloromethane as the extractant in an ordinary manner, an oily residue was obtained. This residue was subjected to the subsequent reaction without the purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396844B1
Source datasetuspto-grants-2008_07
ORD IDord-4018d08373b244ef8b90c7019db12eea
Source noteuspto-grants-2008_07