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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282791Generated: October 31, 2026

Benzyl Bromide → HCID 21520060, compound

https://huagongshe.com/reaction/1282791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21520079HCID 21520079—
SolventWaterHCID 962—
ProductHCID 21520060HCID 21520060—

Reaction Steps

3-Mercapto-4-phenoxy-5-sulfamylbenzoic acid (0.6 g) is suspended in water (20 ml) and the pH is adjusted to 8 by addition of 1 N sodium hydroxide. Benzyl bromide (0.35 g) is added to the resulting solution, and the reaction mixture is stirred for 2 hours at room temperature. After cooling, the precipitated sodium salt of 3-benzylthio-4-phenoxy-5-sulfamylbenzoic acid is collected by filtration. The salt is dissolved in hot water (60 ml) and the solution acidified by addition of 1 N hydrochloric acid. After cooling, the precipitated 3-benzylthio-4-phenoxy-5-sulfamylbenzoic acid is collected by filtration and recrystallized from aqueous ethanol to yield the desired compound with a melting point of 234°-236°C., after drying in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03972886
Source datasetuspto-grants-1976_08
ORD IDord-3bd6afdb58f1402d8ddbd254ab2485cf
Source noteuspto-grants-1976_08