HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Chloro-5-(2-acetamidophenylsulfamoyl)-3-nitrobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Chloro-5-chlorosulfonyl-3-nitrobenzoic acid | HCID 89892 | — |
| Reactant | 2-Aminoacetanilide | HCID 208384 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-5-(2-acetamidophenylsulfamoyl)-3-nitrobenzoic acid | HCID 21558937 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 38.8 g 4-chloro-5-chlorosulfonyl-3-nitrobenzoic acid, 39.9 g of 2-aminoacetanilide and 150 ml of dimethylformamide is stirred for 2 1/2 hours at room temperature. It is poured into 1.7 1t of water and 20 ml of concentrated hydrochloric acid while stirring, the precipitate formed is filtered off and washed with water. It is dissolved in 600 ml of hot ethanol, 900 ml of hot water are added, the mixture filtered and the filtrate left in the cold, to yield the 4-chloro-5-(2-acetamidophenylsulfamoyl)-3-nitrobenzoic acid melting at 225°-227° with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03939267 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-4c61690541e04cdaa53fe8bbb56df48e |
| Source note | uspto-grants-1976_02 |