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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901233Generated: October 30, 2026

Benzyl Chloride → 4-(Chloromethyl)benzene-1-sulfonyl chloride

https://huagongshe.com/reaction/1901233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantChlorosulfonic acidHCID 24638—
Product4-(Chloromethyl)benzene-1-sulfonyl chlorideHCID 22501399—

Reaction Steps

To a 250 mL flask, fitted with addition funnel, reflux condenser and thermometer, is placed 50 g (0.43 mole) of chlorosulfonic acid. Benzyl chloride, (18 g, 0.14 mole) is added to the reaction mixture, slowly, with continuous stirring, over a period of two hours. The temperature of the reaction is kept near room temperature using a water bath. After the addition is complete, the stirring is continued for at least one hour. After analysis by thin layer chromatography shows that the reaction is complete, the reaction mixture is poured into 150 g of crushed ice. The solid is collected and washed with cold water several times. The crude product is further purified by recrystallization. The product is characterized using 1H NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576424
Source datasetuspto-grants-1996_11
ORD IDord-24248eaafa434dfba3e8c13d58f2054d
Source noteuspto-grants-1996_11