HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitro-2-(trifluoromethyl)anisole → 5-Amino-2-methoxybenzotrifluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitro-2-(trifluoromethyl)anisole | HCID 69562 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Amino-2-methoxybenzotrifluoride | HCID 600705 | — |
Reaction Steps
The title compound is prepared from 1-methoxy-4-nitro-2-trifluoromethyl-benzene (1 g, 4.43 mmol) by hydrogenation (5→1.4 bar) in the presence of Raney-Ni (0.3 g) in MeOH (20 mL) during 15 h. The product is isolated by filtration of the reaction suspension over Hyflo and evaporation of the solvent under reduced pressure to give compound of Stage 149.1 as a beige solid: M+H=191.9; Rf (AcOEt/hexane=1:1): 0.33.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652022B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-7d4d8af771c74632be6fb8d76070401e |
| Source note | uspto-grants-2010_01 |