HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethylpyridinium iodide → 1-Methyl-2-[m-(2,2-dimethoxyethoxy)-styryl]pyridinium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethylpyridinium iodide | HCID 70107 | — |
| Reactant | m-(2,2-Dimethoxyethoxy)benzaldehyde | HCID 20572041 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Methyl-2-[m-(2,2-dimethoxyethoxy)-styryl]pyridinium iodide | HCID 70575871 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04287335 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-37d5fd755cec42079094b51892d6723f |
| Source note | uspto-grants-1981_09 |