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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580828Generated: November 3, 2026

Hydrochloric Acid → 4-Chloro-5-(2-acetamidophenylsulfamoyl)-3-nitrobenzoic acid

https://huagongshe.com/reaction/1580828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant4-Chloro-5-chlorosulfonyl-3-nitrobenzoic acidHCID 89892—
Reactant2-AminoacetanilideHCID 208384—
SolventWaterHCID 962—
Product4-Chloro-5-(2-acetamidophenylsulfamoyl)-3-nitrobenzoic acidHCID 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 21/2 hours at room temperature. It is poured into 1.7 lt 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. [In the analogous manner the 5-(4-acetamidophenylsulfamoyl)-isomer is prepared, m.p. 245°-246° (dec.).]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03933906
Source datasetuspto-grants-1976_01
ORD IDord-0ccf42553e5c4925ab0020e4e6555b4a
Source noteuspto-grants-1976_01