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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577287Generated: October 26, 2026

1,2-Dimethylpyridinium iodide → 1-Methyl-2-[m-(2,2-dimethoxyethoxy)-styryl]pyridinium iodide

https://huagongshe.com/reaction/1577287

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dimethylpyridinium iodideHCID 70107—
Reactantm-(2,2-Dimethoxyethoxy)benzaldehydeHCID 20572041—
CatalystPiperidineHCID 8082—
SolventMethanolHCID 887—
Product1-Methyl-2-[m-(2,2-dimethoxyethoxy)-styryl]pyridinium iodideHCID 7057587186%

Reaction Steps

In 6 ml of methanol, 1.50 g of 1,2-dimethyl pyridinium iodide and 1.50 g of m-(2,2-dimethoxyethoxy)-benzaldehyde were dissolved. The resultant solution, with two drops of piperidine added thereto, was refluxed for five hours and thereafter cooled off. Consequently, crystals were deposited. When the crystals were collected and washed thoroughly with acetone, there was obtained 2.34 g of 1-methyl-2-[m-(2,2-dimethoxyethoxy)-styryl]pyridinium iodide. In water, this product showed the highest absorption at 336 nm (ε=2.13×104). The infrared absorption spectrum (KBr) showed peaks at 1620, 1600, 1580, 1268, 1137, 1068, 965, 840, 772 and 680 cm-1. The yield was 86%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04287335
Source datasetuspto-grants-1981_09
ORD IDord-37d5fd755cec42079094b51892d6723f
Source noteuspto-grants-1981_09