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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69432Generated: October 26, 2026

Methanesulfonyl chloride → (S)-1-(tetrahydrofuran-2-yl)methyl methanesulfonate

https://huagongshe.com/reaction/69432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(2S)-(+)-2-(Hydroxymethyl)tetrahydrofuranHCID 637528—
SolventPyridineHCID 1049—
Product(S)-1-(tetrahydrofuran-2-yl)methyl methanesulfonateHCID 18649743—

Reaction Steps

Mesylchloride (12.1 g) was added to a mixture of (S)-1-(Tetrahydro-furan-2-yl)-methanol (10.0 g) and pyridine (55 mL) at −15° C. and stirred for 1.5 hours at room temperature. The mixture was poured into ice water and extracted with ethyl acetate. The organic phase was washed with a solution of potassium hydrogensulfate (20%) and with a solution of saturated sodium hydrogencarbonate, dried over magnesium sulfate and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822495B2
Source datasetuspto-grants-2014_09
ORD IDord-c239c99e0dac47eabc6971ad83b5e709
Source noteuspto-grants-2014_09