HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270137Generated: October 31, 2026
Acetic Acid → methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate
https://huagongshe.com/reaction/2270137
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 | — |
Reaction Steps
50.0 g (0.158 mol) of methyl 2-(N-tert-butylsulfamoyl)-4-nitrobenzoate (prepared according to 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 a little at a time in such a manner that the temperature does not rise above 85° C. The mixture is subsequently stirred at 80° C. for 4 h, 85 ml of 2N HCl are added at this temperature and the mixture is allowed to cool to 25° C. The mixture is filtered off and the solid is washed thoroughly with water. The solid is subsequently 3× extracted hot with in each case 250 ml of ethyl acetate. The ethyl acetate phase is evaporated, and the residue is triturated with diisopropyl ether and dried. This gives 37.7 g (83% of theory) of methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate of m.p. 198-1990° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06331506B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-d29eab2e1cab4fd892e70843f06e0a1f |
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| Source note | uspto-grants-2001_12 |
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