HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Benzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzyl Alcohol | HCID 244 | — |
| Product | Benzylamine | HCID 7504 | 64.6% |
| Product | Benzenemethanamine, N-(phenylmethylene)- | HCID 95831 | 19.3% |
Reaction Steps
To test whether increasing the concentration of ammonia relative to the alcohol might reduce the formation of imines (for example by capturing the contemplated intermediate aldehyde and preventing its reaction with the primary amine), complex 1 (0.01 mmol), benzyl alcohol (2.5 mmol) and ammonia (8 atm) in toluene were heated under reflux in a Fischer-Porter tube for 130 min, to get benzylamine (64.6%) and N-benzylidenebenzylamine (19.3%) whereas the conversion of benzyl alcohol was 84.7% (compare to entry 6, Table 1). Thus, increasing the concentration of ammonia did not affect the extent of formation of imine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889865B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-90461399950e43e49f5694cb1cb97498 |
| Source note | uspto-grants-2014_11 |