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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580826Generated: November 4, 2026

Acetic Anhydride → HCID 21563919, compound

https://huagongshe.com/reaction/1580826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 21563902HCID 21563902—
ProductHCID 21563919HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03933906
Source datasetuspto-grants-1976_01
ORD IDord-d9adb73cd0a049eab607d34f1e4e661b
Source noteuspto-grants-1976_01