HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethylpyridinium iodide → 1-Methyl-2-[o-(2,2-dimethoxyethoxy)-styryl]pyridinium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethylpyridinium iodide | HCID 70107 | — |
| Reactant | 2-(2,2-Dimethoxyethoxy)benzaldehyde | HCID 20572034 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Methyl-2-[o-(2,2-dimethoxyethoxy)-styryl]pyridinium iodide | HCID 70575863 | 87% |
Reaction Steps
In 6 ml of methanol, 1.50 g of 1,2-dimethylpyridinium iodide and 1.50 g of o-(2,2-dimethoxyethoxy)benzaldehyde. The resultant solution, with two drops of piperidine added thereto, was refluxed for five hours and then left to stand and cool off. The crystals which deposited consequently were collected and thoroughly washed with acetone. Consequently, there was obtained 2.36 g of 1-methyl-2-[o-(2,2-dimethoxyethoxy)-styryl]pyridinium iodide which melted at 169°~173° C. This product showed the highest absorption at 353 nm (ε=1.78×104). The infrared absorption spectrum (KBr) showed peaks at 1630, 1610, 1595, 1567, 1515, 1500, 1450, 1280, 1248, 1130, 1065, 971, 780, 760 and 750 cm-1. The yield was 87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04287335 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-ec75d7a706e44f4081940988e2de3279 |
| Source note | uspto-grants-1981_09 |