HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(4-Acetamidophenoxy)-3-nitro-5-sulfamoylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetaminophen | HCID 1983 | — |
| Reactant | 4-Chloro-3-nitro-5-sulphamoylbenzoic acid | HCID 89893 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 4-(4-Acetamidophenoxy)-3-nitro-5-sulfamoylbenzoic acid | HCID 21497789 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 14 g of 4-chloro-3-nitro-5-sulfamoylbenzoic acid, 200 ml of 1N aqueous sodium bicarbonate and 15.9 g of 4-acetamidophenol is heated to about 95°-100°C for 21 hours while stirring under nitrogen. It is cooled to room temperature and made strongly acidic with concentrated hydrochloric acid. The precipitate formed is filtered off, to yield the 4-(4-acetamidophenoxy)-3-nitro-5-sulfamoylbenzoic acid, which after trituration with aqueous ethanol melts at 293° with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03982018 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-af303161c4ac41ea9fc014a5dec651ae |
| Source note | uspto-grants-1976_09 |