HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-nitro-3-(trifluoromethyl)benzenesulfonamide → HCID 21482732, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-nitro-3-(trifluoromethyl)benzenesulfonamide | HCID 2778406 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21482732 | HCID 21482732 | — |
Reaction Steps
1.0 G. of 4-nitro-3-trifluoromethylbenzenesulfonamide is hydrogenated over 5% Ruthenium on charcoal in 20 ml. of absolute ethanol at room temperature under 40 lbs. of hydrogen for 5 hours. The hydrogen uptake is 100% of theory. The mixture is filtered, evaporated and dried affording 0.87 g. of crude solid. This material is recrystallized from toluene affording 0.75 g. of 4-amino-3-trifluoromethylbenzenesulfonamide, m.p. 150° to 151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03987199 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-caf80078ef27423ebbba1078e8e7c7fa |
| Source note | uspto-grants-1976_10 |