HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21563919, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 21563902 | HCID 21563902 | — |
| Product | HCID 21563919 | HCID 21563919 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 20 g of 4-(4-acetamidophenylamino)-3-nitro-5-sulfamoylbenzoic acid and 200 ml of acetic anhydride is refluxed for ten minutes while stirring under nitrogen. It is evaporated under reduced pressure, the residue triturated with water and dissolved in 200 ml of 2N aqueous sodium hydroxide. The solution is washed with diethyl ether, filtered and acidified with concentrated hydrochloric acid to pH of 1- and the precipitate filtered off, to yield the 4-(4-acetamidophenylamino)-3-nitro-5-acetylsulfamoylbenzoic acid melting at 175°-185°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03933906 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-d9adb73cd0a049eab607d34f1e4e661b |
| Source note | uspto-grants-1976_01 |