HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha,alpha,alpha-Trifluoro-3-nitro-4-(phenylthio)toluene → 2-(Phenylsulfanyl)-5-(trifluoromethyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha,alpha,alpha-Trifluoro-3-nitro-4-(phenylthio)toluene | HCID 67667 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Phenylsulfanyl)-5-(trifluoromethyl)aniline | HCID 12590363 | — |
Reaction Steps
26.9 g of 3-nitro-4-(phenylthio)-benzotrifluoride in 250 ml of ethanol are hydrogenated in the presence of 10 g of Raney-nickel at room temperature and atmospheric pressure for 17 hours. The mixture is filtered and evaporated under reduced pressure. There is obtained 3-amino-4-(phenylthio)-benzotrifluoride as a red-brown oil. The compound is distilled under greatly reduced pressure and boils at 110°-135° C/0.1 mm; orange-coloured oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006144 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-05f2fc180ce546d7bad93d597545d791 |
| Source note | uspto-grants-1977_02 |