HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitro-4-phenyl-5-sulfamylbenzoic acid → 3-Amino-4-phenyl-5-sulfamylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitro-4-phenyl-5-sulfamylbenzoic acid | HCID 21546843 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Palladium | HCID 23938 | — |
| Product | 3-Amino-4-phenyl-5-sulfamylbenzoic acid | HCID 21546841 | — |
Reaction Steps
To a solution of 3-nitro-4-phenyl-5-sulfamylbenzoic acid (8.5 g) in acetic acid (100 ml), palladium (10%) on carbon (1.5 g) is added, and the mixture is hydrogenated. After 2-2.5 hours the theoretical amount of hydrogen has been absorbed, and the hydrogen uptake has subsided. The catalyst is removed by filtration, and the filtrate is evaporated in vacuo. The residue is recrystallized from acetic acid to give 3-amino-4-phenyl-5-sulfamylbenzoic acid with a melting point of 232.5°-237° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03950380 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-8cf6a0da7ddb42d4960d7d943f93761f |
| Source note | uspto-grants-1976_04 |