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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046355Generated: October 30, 2026

Water → 1-(Chloromethyl)-3-methanesulfonylbenzene

https://huagongshe.com/reaction/1046355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(3-Methanesulfonylphenyl)methanolHCID 23549738—
SolventDichloromethaneHCID 6344—
Product1-(Chloromethyl)-3-methanesulfonylbenzeneHCID 22050411—

Reaction Conditions

Temperature50 °C

Reaction Steps

0.267 ml (3.45 mmol) methanesulphonyl-chloride is added to o a solution of 584 mg (3.14 mmol) (3-methanesulphonyl-phenyl)-methanol and 0.66 ml (4.71 mmol) triethylamine in 6 ml dichloromethane. This reaction mixture is stirred at room temperature for 1 h and at 50° C. for additional 3 h. The reaction mixture is then poured into water and extracted twice with dichloromethane. The combined organic layers are washed with water and brine, dried, filtered and concentrated in vacuo to afford the title compound, which is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569317B2
Source datasetuspto-grants-2013_10
ORD IDord-1c147eb4a0404258b46998e02b250b47
Source noteuspto-grants-2013_10