HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Trifluoromethylphenylacetonitrile → Phenethylamine, m-trifluoromethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Trifluoromethylphenylacetonitrile | HCID 75360 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ammonia | HCID 222 | — |
| Product | Phenethylamine, m-trifluoromethyl- | HCID 104223 | 97.89% |
Reaction Steps
Using analogous reaction conditions as described in Example 16, step 1, (3-trifluoromethyl-phenyl)-acetonitrile (2 g, 10.81 mmol) in methanolic ammonia (50 mL) was reacted with to Raney nickel (400 mg) to afford 2 g of the product (97.89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946260B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-73b033b232a74f7087ac7a53ba2ff886 |
| Source note | uspto-grants-2015_02 |