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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419202Generated: November 1, 2026

Benzoyl chloride → 4-Benzamido-1-(2-benzoyloxyethyl)piperidine

https://huagongshe.com/reaction/2419202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant1-(2-Hydroxyethyl)-4-benzamidopiperidineHCID 20315176—
SolventDichloromethaneHCID 6344—
Product4-Benzamido-1-(2-benzoyloxyethyl)piperidineHCID 2031517575%

Reaction Steps

1.4 Milliliters (0.012 mol) of benzoylchloride were added to a stirred solution of 2.48 grams (0.01 mol) of 4-benzamido-1-(2-hydroxyethyl)piperidine and 2.8 milliliters (0.02 mol) of triethylamine in 10 milliliters of dichloromethane. The solution was stirred at room temperature for 2 hours, then washed with water, dried and evaporated. The residue was crystallised from n-butyl acetate to give 2.5 grams (75% yield) of the title compound m.p. 139°-40° C. Treatment of a solution of the base in ethanol with ethanolic hydrogen chloride precipitated the hydrochloride, m.p. 217°-18° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105666
Source datasetuspto-grants-1978_08
ORD IDord-56f7d3a66bf24851ad457838c707d613
Source noteuspto-grants-1978_08