Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653199Generated: October 28, 2026

Acetone → Encainide hydrochloride

https://huagongshe.com/reaction/653199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactantp-Anisoyl chlorideHCID 7477—
Reactant2-(2-Aminophenethyl)-1-methylpiperidineHCID 11085282—
ReactantHCID 85370880HCID 85370880—
CatalystPlatinumHCID 23939—
SolventAcetonitrileHCID 6342—
SolventPotassium AcetateHCID 517044—
ProductEncainide hydrochlorideHCID 48040—

Reaction Steps

A process for preparing 4-methoxy-2'-[2-(1-methyl-2-piperidyl) ethyl]benzanilide (I) as the hydrochloride salt ##STR4## which comprises (a) combining α-picoline and dimethylsulfate to form the picolinium methyl sulfate salt (V) ##STR5## which is then reacted with o-nitrobenzaldehyde to produce 1-(2-nitrophenyl)-2-[2-1-methyl) pyridinium methyl sulfate]-ethanol (IV) ##STR6## (b) dehydrating (IV) by heating in a mixture of acetic acid, acetic anhydride and potassium acetate to yield 2-(2-nitrostyrenyl)-[2-(1-methyl) pyridinium methyl sulfate ] (III); ##STR7## (c) hydrogenating (III) using a platinum catalyst to generate 2-(2-aminophenethyl)-1-methylpiperidine (II); and ##STR8## (d) reacting (II) with anisoyl chloride in an organic solvent selected from the group consisting of acetone, acetonitrile, and a C2-5 alkanol, to obtain encainide hydrochloride directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04675409
Source datasetuspto-grants-1987_06
ORD IDord-9f54906643bf4aa6ba48a5c9575ef91f
Source noteuspto-grants-1987_06