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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616028Generated: October 31, 2026

Benzene → 1-[3-(3,4-Dimethoxyphenyl)piperidin-1-yl]ethan-1-one

https://huagongshe.com/reaction/616028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(3,4-Dimethoxyphenyl)piperidineHCID 12937921—
SolventWaterHCID 962—
Product1-[3-(3,4-Dimethoxyphenyl)piperidin-1-yl]ethan-1-oneHCID 20370846—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 8 g of 3-(3',4'-dimethoxyphenyl)-piperidine, 80 ml of benzene and 3.6 ml of acetic acid anhydride was stirred at 20° C for an hour and was then diluted with 100 ml of water. 500 ml of an aqueous solution saturated with sodium bicarbonate were added thereto and the mixture was stirred for an hour and then was decanted. The aqueous phase was re-extracted with ethyl acetate and the organic phases were washed with water, dried and evaporated to dryness. The residue was chromatographed over silica gel and was eluted with a 6-3-1 cyclohexane-chloroform-triethylamine mixture to obtain 6.75 g of N-acetyl-3-(3',4'-dimethoxyphenyl)-piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072685
Source datasetuspto-grants-1978_02
ORD IDord-6f0d9fe2863b4bd78b212c160161ff3c
Source noteuspto-grants-1978_02