HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 70577732, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1,2-Dimethylquinolinium iodide | HCID 2750445 | — |
| Reactant | p-(2,2-Dimethoxyethoxy)benzaldehyde | HCID 20572032 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70577732 | HCID 70577732 | 70.2% |
Reaction Steps
In 20 ml of methanol, 4.28 g of 1,2-dimethylquinolinium iodide and 3.47 g of p-(2,2-dimethoxyethoxy)benzaldehyde were dissolved. The resultant solution, with 0.3 ml of piperidine added thereto, was refluxed for seven hours. The solution was left to cool. The crystals which consequently deposited were collected through filtration and then washed thoroughly with acetone. Consequently, there was obtained 5.03 g of 1-methyl-2-[p-(2,2-dimethoxyethoxy)-styryl]quinolinium iodide which boiled at 209°~212° C. This product in water showed absorption bands (λmax) at 224, 255, 307 and 399 nm. The infrared absorption spectrum (KBr) showed peaks at 1610, 1590, 1572, 1516, 1240, 1180, 1130, 1068, 985, 830, 780 and 760 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04287335 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-d3525303220a497a8b7fb5e8686c6147 |
| Source note | uspto-grants-1981_09 |