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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768721Generated: October 31, 2026

Triethylamine → Benzyl 4-Hydroxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/1768721

Reaction equation

Participants

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

Reaction Steps

69.1 ml of triethylamine and 70.2 ml of benzyl chloroformate are added in succession at 0° C. to a solution of 50 g of 4-hydroxypiperidine in 500 ml of dichloromethane. The resulting suspension is stirred at room temperature overnight and subsequently filtered. The residue which separates after concentration of the filtrate is taken up in ethyl acetate, washed with water and 1N hydrochloric acid, dried and concentrated. There are obtained 73.6 g of N-benzyloxycarbonyl-4-hydroxy-piperidine. Rf =0.56 (ethyl acetate/methanol 9:1), MS (EI): 235 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378712
Source datasetuspto-grants-1995_01
ORD IDord-bbc82c01f6714546a39520fd71994fb0
Source noteuspto-grants-1995_01