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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46582Generated: October 26, 2026

Acetone → 3-(3-Bromophenyl)-4-methoxy-1-methyl-5-phenylpyridinium trifluoromethanesulfonate

https://huagongshe.com/reaction/46582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant2-PyridoneHCID 8871—
ReactantMethyl triflateHCID 9526—
Reactant3-(3-Bromophenyl)-1-methyl-5-phenylpyridin-4(1H)-oneHCID 12879275—
SolventChloroformHCID 6212—
Product3-(3-Bromophenyl)-4-methoxy-1-methyl-5-phenylpyridinium trifluoromethanesulfonateHCID 23345772—

Reaction Steps

A 10 g. portion of 3-(3-bromophenyl)-1-methyl-5-phenyl-4(1H)-pyridinone was made from 22 g. of the corresponding 2-propanone as described in Example 1. A 3.4 g. portion of the intermediate pyridinone was dissolved in chloroform and 1.8 g. of methyl trifluoromethanesulfonate was added. The reaction mixture was allowed to stand overnight, and the volatile portions were then evaporated under vacuum. The residue was identified as 3-(3-bromophenyl)-4-methoxy-1-methyl-5-phenylpyridinium trifluoromethanesulfonate, molecular weight 339 by mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174209
Source datasetuspto-grants-1979_11
ORD IDord-b4933e6ff4514b2a8f47b2d1faa81725
Source noteuspto-grants-1979_11