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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587329Generated: October 30, 2026

Acetic Anhydride → trans Ethyl 1-acetyl-4-(2-hydroxyethyl)-piperidine-2-carboxylate

https://huagongshe.com/reaction/1587329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl 4-(2-hydroxyethyl)piperidine-2-carboxylateHCID 19757829—
SolventPyridineHCID 1049—
Producttrans Ethyl 1-acetyl-4-(2-hydroxyethyl)-piperidine-2-carboxylateHCID 14541466—

Reaction Steps

At 0°, 9.4 ml acetic anhydride is added to a stirred solution of 13.5 g of ethyl 4-(2-hydroxyethyl)-piperidine-2-carboxylate in 75 ml pyridine. After stirring at room temperature for 30 minutes the solution is concentrated in vacuo and ethyl acetate (300 ml) is added; the solution is washed twice with 2N hydrochloric acid, once with water and once with saturated sodium bicarbonate, dried over sodium sulfate, filtered and concentrated in vacuo. The residue is dissolved in 100 ml ethanol, 5 g of powdered potassium carbonate is added and the mixture stirred 1 hour at room temperature. The solution is filtered, concentrated in vacuo and purified by flash chromatography using methylene chloride/methanol (95:5) to yield trans ethyl 1-acetyl-4-(2-hydroxyethyl)-piperidine-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217963
Source datasetuspto-grants-1993_06
ORD IDord-36c20943a4f44cf59060f13371d5f420
Source noteuspto-grants-1993_06