HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076767Generated: October 25, 2026
Sulfamic Acid → 2-Amino-4-methyl-5-nitrobenzenesulfonic acid
https://huagongshe.com/reaction/1076767
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | 4-Nitro-m-toluidine | HCID 11898 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-Amino-4-methyl-5-nitrobenzenesulfonic acid | HCID 3016283 | — |
Reaction Steps
18.3 g of 1-amino-3-methyl-4-nitrobenzene, 120 ml of chlorobenzene, 24 g of sulphamic acid and 12 ml of 1-methylpyrrolid-2-one are warmed to 120°C whilst stirring. The reaction mixture is stirred for 8 hours at this temperature. After cooling, the reaction mixture is filtered and the residue is washed with trichloroethylene and recrystallised from 200 ml of water. The crystals which have precipitated are filtered off, suspended in 100 ml of trichloroethylene, stirred for one hour at 75°C, separated from the organic solvent by filtration and dried at 80°C. 25 g (84% of theory) of yellow crystals, which according to thin layer chromatography are a single substance, of 1-amino-3-methyl-4-nitro-benzene-6 -sulphonic acid in the form of its ammonium salt [melting point 290° C (decomposition)]are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03957860 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-be9aab24b5504072bd01e51661a3a3ab |
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| Source note | uspto-grants-1976_05 |
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