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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577288Generated: October 25, 2026

Piperidine → HCID 70576684, compound

https://huagongshe.com/reaction/1577288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1,2-Dimethylpyridinium iodideHCID 70107—
ReactantHCID 20572032HCID 20572032—
SolventMethanolHCID 887—
ProductHCID 70576684HCID 7057668470.6%

Reaction Steps

In 50 ml of methanol, 12.7 g of 1,2-dimethylpyridinium iodide and 11.96 g of p-(2,2-dimethoxyethoxy)benzaldehyde were dissolved. The resultant solution, with 1 ml of piperidine added thereto, was refluxed for five hours. The solution was left to cool and the crystals which consequently deposited in the solution were collected through filtration and thoroughly washed with acetone. Consequently, there was obtained 16.30 g of 1-methyl-2[p-(2,2-dimethoxyethoxy)-styryl]pyridinium iodide. In water, this product showed the highest absorption at 360 nm (ε=2.67×104). The infrared absorption spectrum (KBr) of the product showed peaks at 1630, 1615, 1595, 1568, 1512, 1450, 1298, 1260, 1180, 1140, 1073, 965, 862, 821 and 776 cm-1. The yield was 67%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04287335
Source datasetuspto-grants-1981_09
ORD IDord-72bc878b0a964798bd0c73169da3ba30
Source noteuspto-grants-1981_09