HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-[4-(Trifluoromethoxy)phenyl]ethan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-(Trifluoromethoxy)phenylacetonitrile | HCID 142676 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[4-(Trifluoromethoxy)phenyl]ethan-1-amine | HCID 10632040 | — |
Reaction Steps
650 ml of methanol, 260 g of (4-trifluoromethoxyphenyl)acetonitrile, and moist Raney nickel in an amount corresponding to 0.39 mol were initially charged in an autoclave, and 260 ml of ammonia were condensed in. The mixture was hydrogenated at 130° C. and a hydrogen pressure of 140 bar for 2 hours. The reaction mixture was then vented at room temperature, and the catalyst was filtered off. The filtrate was distilled at 10 hPa. This gave 224.5 g of 2-(4-trifluoromethoxyphenyl)ethylamine as a colorless liquid (86.7% of theory) of b.p. 84-86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441239B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-bf724499115d4aee807d3dd83af1bacf |
| Source note | uspto-grants-2002_08 |