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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926127Generated: November 3, 2026

Water → 4-{[Tert-butyl(dimethyl)silyl]oxy}but-2-yn-1-yl methanesulfonate

https://huagongshe.com/reaction/1926127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-((Tert-butyldimethylsilyl)oxy)but-2-yn-1-olHCID 5461845—
SolventEthyl AcetateHCID 8857—
Product4-{[Tert-butyl(dimethyl)silyl]oxy}but-2-yn-1-yl methanesulfonateHCID 86615779—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-{[Tert-butyl(dimethyl)silyl]oxy}but-2-yn-1-ol (701.4 mg) was dissolved in ethyl acetate (15 mL), and the solution was cooled to 0° C. Triethylamine (1.1 mL) and methanesulfonyl chloride (0.3 mL) were added, and the mixture was stirred at 0° C. for 3 hrs. Water was added to the reaction mixture and the mixture was extracted with diethyl ether. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was separated and purified by silica gel column chromatography (eluent, hexane:ethyl acetate=90:10→50:50) to give the title compound (469.7 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-f67e0c5573474a96a6a9e38a940f11f0
Source noteuspto-grants-2012_05