HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581655Generated: October 25, 2026
Acetic Acid → methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate
https://huagongshe.com/reaction/581655
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | methyl 2-(N-tert-butylsulfamoyl)-4-nitrobenzoate | HCID 15240542 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate | HCID 10946074 | 83.3% |
Reaction Steps
50.0 g (0.158 mol) of methyl 2-(N-tert-butylsulfamoyl)-4-nitrobenzoate (prepared in accordance with DE-OS 4 236 902) are added to a mixture of 180 ml of acetic acid and 75 ml of water and the mixture is heated to 80° C. 26.5 g (0.474 mol) of iron powder are added in portions such that the temperature does not rise above 85° C. The mixture is then stirred at 80° C. for 4 hours, 85 ml of 2N HCl are added at this temperature and the mixture is allowed to cool to 25° C. The solid is filtered off and washed thoroughly with water. It is then extracted hot 3 times with 250 ml of ethyl acetate each time. The ethyl acetate phase is evaporated and the residue is triturated with diisopropyl ether and dried. 37.7 g (83% of theory) of methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate of melting point 198-199° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922645 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-c3a8ecc33de4441cb44045ddec8c755a |
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| Source note | uspto-grants-1999_07 |
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