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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308757Generated: November 1, 2026

Acetonitrile → HCID 20187494, compound

https://huagongshe.com/reaction/2308757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant4-BenzylpiperidineHCID 31738—
ReactantHCID 20187481HCID 20187481—
SolventDiethyl EtherHCID 3283—
ProductHCID 20187494HCID 20187494—

Reaction Conditions

Temperature0 °C

Reaction Steps

21 g of 2-bromo-3'-,5'-dimethylpropiophenone are introduced into 50 ml of acetonitrile, the mixture is cooled to 0° C., 30.5 g of 4-benzylpiperidine are added and the mixture is stirred for 3 hours. It is diluted with 30 ml of diethyl ether, the precipitated hydrobromide is filtered off and 150 ml of diethyl ether are added to the filtrate, which produces a second crop of precipitate. This is filtered off and the filtrate is treated twice with 200 ml of 3N hydrochloric acid. The diethyl ether phase is separated off. The aqueous phase contains the hydrochloride of the propiophenone formed, as an emulsion. This aqueous phase is extracted with methylene chloride, the organic phase obtained is washed with water, dilute aqueous ammonia solution is added, the organic phase is decanted, washed with water, dried, filtered and treated with 100 g of silica, the mixture is filtered and the filtrate is evaporated. 14.4 g of an oil remain.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04690931
Source datasetuspto-grants-1987_09
ORD IDord-8d3798cc60c9498db80ed06035fe512c
Source noteuspto-grants-1987_09