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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179646Generated: October 31, 2026

Methanesulfonyl chloride → 2-(3-Iodophenyl)ethyl methanesulfonate

https://huagongshe.com/reaction/1179646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(3-Iodophenyl)ethanolHCID 15169850—
SolventDichloromethaneHCID 6344—
SolventAmmonium ChlorideHCID 25517—
Product2-(3-Iodophenyl)ethyl methanesulfonateHCID 5744437045%

Reaction Steps

Methanesulfonyl chloride (1.5 mL, 1.2 eq.) was added dropwise to a stirred solution of 2-(3-iodophenyl)ethanol (3.6 g) in dichloromethane (100 mL) and diisopropylethylamine (3.8 mL, 1.5 equiv.) at 0° C. The solution was warmed to room temperature and stirred for 18 h. The reaction mixture was diluted with aqueous ammonium chloride solution and extracted with dichloromethane. The organic layers were combined, washed with aqueous sodium hydrogencarbonate solution, brine, dried over sodium sulfate and concentrated under reduced pressure. The crude was purified using column chromatography (SiO2 cartridge) using DCM-cyclohexane (70:30) to afford the title compound (3.2 g, 45% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279481B2
Source datasetuspto-grants-2007_10
ORD IDord-435a526d00724656b7b645ebf86ef824
Source noteuspto-grants-2007_10