HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Dibenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorous acid | HCID 107909 | — |
| Solvent | Water | HCID 962 | — |
| Product | Dibenzylamine | HCID 7656 | 98% |
Reaction Steps
The imine from benzaldehyde and benzylamine (19.5 g; 0.1 mole) was heated with phosphorous acid (8.2 g; 0.1 mole) and triethylamine (10.1 g; 0.1 mole) for 2 hours at reflux (125°-130°). After cooling to 90° the reaction mixture was diluted with water (50 ml), basified (NaOH) and extracted with chloroform. The extract was concentrated by evaporation of the chloroform and triethylamine to yield dibenzylamine 19.3 g (98% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04442286 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-275c7b0824a14fd9a2f2fc6043d61885 |
| Source note | uspto-grants-1984_04 |