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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237490Generated: October 29, 2026

Methanesulfonyl chloride → HCID 18343025, compound

https://huagongshe.com/reaction/237490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-HydroxyazetidineHCID 1514290—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18343025HCID 18343025—

Reaction Conditions

Temperature0 °C

Reaction Steps

Azetidin-3-ol (3.3 g) and DIPEA (20 mL) are dissolved in dry tetrahydrofuran (40 mL). After 30 min the reaction mixture is cooled to 0° C. and methanesulfonyl chloride (10.9 g) is added dropwise. After stirring for 2 hours at ambient temperature, the mixture is concentrated under vacuum, partitioned between ethyl acetate and water. The organic phase is dried (MgSO4) and concentrated. Chromatography of the residue on silica gel (cyclohexane/ethyl acetate 70:30) gives the title compound. Yield: 5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642585B2
Source datasetuspto-grants-2014_02
ORD IDord-abacf6cbd49b40a4aa0a39b0168661ae
Source noteuspto-grants-2014_02