HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → N-[(4-chloro-2-methylphenyl)-methylene]benzeneamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 4-Chloro-2-methylbenzaldehyde | HCID 2757658 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[(4-chloro-2-methylphenyl)-methylene]benzeneamine | HCID 13553333 | 77% |
Reaction Steps
A mixture of 4-chloro-2-methylbenzaldehyde (3.5 g, 22.6 mmol) and aniline (2.11 g, 22.6 mmol) in toluene (40 ml) was heated at reflux in a Dean-Stark apparatus for 1 hour. The mixture was cooled and evaporated in vacuo to leave an oily residue. The residue was redissolved in ether, washed with 5% sodium bicarbonate solution. The organic phase was separated, dried over MgSO4 and filtered. The filtrate was concentrated in vacuo to afford an oily residue which was purified by distillation via a Kugelrohr apparatus (oven temperature 160° C., 0.5 mm) to provide the title compound (4.0 g, 7.4 mmol, 77%) as a viscous oil; pmr (CDCl3)δ2.5(3H, s), 6.3-7.5(7H,m), 7.95(H, d), 8.6(H,s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04375475 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-37bfeadaa64e48a3b4536a3e202c3f49 |
| Source note | uspto-grants-1983_03 |