HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792765Generated: November 3, 2026
Methylamine → 4-amino-N-methylbenzene-1-sulfonamide
https://huagongshe.com/reaction/1792765
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Aminobenzenesulfonyl fluoride | HCID 66823 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-amino-N-methylbenzene-1-sulfonamide | HCID 74368 | 78.1% |
Reaction Steps
Methylamine (3 ml of a 33% solution in ethanol) and then triethylamine (0.159 ml, 1.1 mmol) was added to sulphanilyl fluoride (200 mg, 1.1 mmol), and the mixture heated at 80° C. for 6 hours then at ambient temperature for 18 hours. The volatiles were removed by evaporation and the residue azeotroped with toluene to give the title compound (160 mg, 76% yield). NMR: 2.30 (s, 3H), 5.85 (s, 2H), 6.60 (d, 2H), 7.39 (d, 2H); m/z: 187 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07078410B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-12f713cbd2b6455fa7fff07a664a3769 |
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| Source note | uspto-grants-2006_07 |
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