HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Trifluoromethylthio)nitrobenzene → 4-((Trifluoromethyl)thio)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Trifluoromethylthio)nitrobenzene | HCID 4210035 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-((Trifluoromethyl)thio)aniline | HCID 123054 | — |
Reaction Steps
To p-nitrophenyl trifluoromethyl sulfide (3.0 g) in absolute ethanol (30 ml) is added Adams catalyst (Pt2O, 0.026 g). The mixture is hydrogenated in a Parr vessel at 50 lbs/sq. in. for about 15 min. The reaction is worked up by filtering through Celite and evaporating to yield p-aminophenyl trifluoromethyl sulfide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04411912 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-1746313fa2d346c3bcf9719c18b8d492 |
| Source note | uspto-grants-1983_10 |