HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (4-aminophenyl)-N-methylmethylenesulfonamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-Methyl-1-(4-nitrophenyl)methanesulfonamide | HCID 703312 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium monoxide | HCID 5083724 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-aminophenyl)-N-methylmethylenesulfonamide hydrochloride | HCID 14234262 | — |
Reaction Steps
A suspension of N-methyl-4-nitrobenzenemethanesulphonamide (30 g) in ethanol (150 ml), water (300 ml) and hydrochloric acid (2N, 65 ml) was hydrogenated over 10% palladium oxide on charcoal (7.5 g, 50% paste with water) until hydrogen uptake ceased (9.75 l). The catalyst was removed by filtration through "hyflo" and the filter pad was washed with water (30 ml). The filtrate was evaporated under reduced pressure to give the title compound as a pale yellow powder (28.2 g) m.p. 143°-144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816470 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-ccdbfabfb80947ddaf33b139441bf3e6 |
| Source note | uspto-grants-1989_03 |