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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730416Generated: November 2, 2026

Benzyl Chloride → HCID 21497805, compound

https://huagongshe.com/reaction/1730416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium HydroxideHCID 14798—
Reactant4-(4-Acetamidophenoxy)-3-amino-5-sulfamoylbenzoic acidHCID 21497838—
SolventWaterHCID 962—
ProductHCID 21497805HCID 21497805—

Reaction Steps

The starting material is prepared as follows: To the mixture of 3.6 g of 4-(4-acetamidophenoxy)-3-amino-5-sulfamoylbenzoic acid, 10 ml of water andthe sufficient amount of N aqueous sodium hydroxide to reach a pH = 7.4, 1.3 g of benzyl chloride are added while stirring at 30°. The mixture is stirred for 16 hours at room temperature, during which time 4N aqueous sodium hydroxide is added dropwise to keep said pH value. It is filtered, the filtrate acidified with glacial acetic acid and the precipitate formed filtered off, to yield the 4-(4-acetamidophenoxy)-3-benzylamino-5-sulfamoylbenzoic acid which, on recrystallization from aqueous ethanol, melts at 255° with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03992440
Source datasetuspto-grants-1976_11
ORD IDord-d2154d7323f3458a8ce7690908c3c5ec
Source noteuspto-grants-1976_11