HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Benzylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Aniline | HCID 6115 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Benzylaniline | HCID 66028 | — |
Reaction Steps
Benzaldehyde(31.84 g, 0.300 mol) and aniline (27.94 g, 0.300 mol) in benzene (100 ml) were heated to remove the water using a Dean-Stark trap. After 5.4 ml of water had been collected, the benzene was stripped off and the residual oil poured into a beaker. On treating with petroleum ether (10-20 ml) the oil crystallized. This mass was suction filtered and washed with some additional petroleum ether. Recrystallization from hexane gave off-white needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196606 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-fb0d45b55f2446ae82b4dd4b1e1989fd |
| Source note | uspto-grants-1993_03 |