HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → p-n-Tetradecyloxy-4-(2-methylbutoxycarbonyl)benzylideneaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | p-(n-Tetradecyloxy)phenylamine | HCID 191002 | — |
| Reactant | p-(2-Methylbutoxycarbonyl)benzaldehyde | HCID 13548338 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | p-n-Tetradecyloxy-4-(2-methylbutoxycarbonyl)benzylideneaniline | HCID 13628479 | — |
Reaction Steps
44.3 g of said p-(2-methylbutoxycarbonyl)benzaldehyde, 32 g of p-n-tetradecyloxyaniline, and 0.1 g of p-toluenesulfonic acid were dissolved in toluene. The solution was heated under reflux, and water generated in the dehydrating condensation was removed with a Dean-Stark condenser. After the reaction solution was cooled, the organic layer was washed with water, and the solvent (toluene) was distilled off in vacuum. The solid residue was recrystallized from ethanol to obtain yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04576732 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-063c506506db4d19beb5dc80ac421b83 |
| Source note | uspto-grants-1986_03 |