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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053967Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86730300, compound

https://huagongshe.com/reaction/1053967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86730301HCID 86730301—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86730300HCID 86730300—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-hydroxytetrahydrothiophene-3-carbonitrile (1.0 g, 7.7 mmol) in DCM (15 mL) was stirred at 0° C. TEA (4.3 mL, 31 mmol) was added followed by the dropwise addition of methanesulfonyl chloride (1.77 g, 15.5 mmol). The resulting mixture was stirred at 0° C. for 30 minutes then warmed to ambient temperature and stirred for an additional 30 minutes. The mixture was carefully diluted with water and extracted with DCM (2×). The combined organic extracts were washed with 1N aqueous HCl, brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The crude residue was purified by MPLC on silica gel (using a gradient elution of 0-5% MeOH/DCM) to afford the title compound, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394282B2
Source datasetuspto-grants-2016_07
ORD IDord-6b6f60c240584a4fa845607064e75263
Source noteuspto-grants-2016_07