HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 5-t-butyl-2-methoxy-3-aminophenyl N-t-butyl sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 5-t-butyl-2-methoxy-3-nitrophenyl N-t-butyl sulfonamide | HCID 15029585 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-t-butyl-2-methoxy-3-aminophenyl N-t-butyl sulfonamide | HCID 15029586 | 94.5% |
Reaction Steps
Ammonium formate (8.0 g) was added to a stirred and cooled mixture of 5-t-butyl-2-methoxy-3-nitrophenyl N-t-butyl-sulfonamide (8.0 g) and 10% Palladium on charcoal (1.1 g) in dry methanol (80 ml) under nitrogen. The mixture was stirred at ambient temperature for 1 hour and then filtered through diatomaceous earth. The filtrate was concentrated and taken up into a mixture of ethyl acetate and water. The organic layer was separated and dried over sodium sulphate. After removal of solvent and recrystallization from aqueous ethanol the title compound was obtained as white crystals (6.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04929269 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-60259e4b53de4df2a0f4a52402df0d5c |
| Source note | uspto-grants-1990_05 |