HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414800Generated: November 1, 2026
N-Methyl-4-nitrobenzenesulfonamide → 4-amino-N-methylbenzene-1-sulfonamide
https://huagongshe.com/reaction/2414800
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methyl-4-nitrobenzenesulfonamide | HCID 232993 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-amino-N-methylbenzene-1-sulfonamide | HCID 74368 | — |
Reaction Steps
To a solution of N-methyl-4-nitrobenzenesulfonamide (Step 5) (4.8 g, 22.2 mmol) in methanol (100 ml) in a Parr bottle was added Raney-nickel in methanol. The reaction mixture was flushed with nitrogen and hydrogen several times and maintained under hydrogen at delivery pressure of 5 psi. After stirring at 25° C. for approximately 20 hr, the reaction was vented and purged with nitrogen. The contents of the reaction were filtered and concentrated to remove the solvent. The 4-[(N-methylamino)sulfonyl]aniline obtained as a white solid (4.1 g, 100%) was used in the next step without further purification: mp (DSC) 138° C. Anal Calc'd. for C7H10N2O2S 0.25 H2O: C, 44.08; H, 5.55; N, 14.69. Found: C, 43.83; H, 5.39; N, 14.81.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06815460B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-dc53b0c26537497a98b9c7f7ac4021dc |
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| Source note | uspto-grants-2004_11 |
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