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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384054Generated: October 27, 2026

tert-Butanol → tert-Butyl ethynsulfonate

https://huagongshe.com/reaction/1384054

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
ReactantHCID 178462451HCID 178462451—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl ethynsulfonateHCID 85699463—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of ethynylmagnesium chloride in THF (0.5M, 10 mmol) is added to a solution of sulfuryl chloride (20 mmol) in 100 mL of THF cooled to −78° C. After 1 hour, a solution of tert-butanol (60 mmol) and triethylamine (60 mmol) in 50 mL of THF is added dropwise. The solution is allowed to warm to room temperature, the volatile components are evaporated in vacuo, the residue is partitioned between ether (150 mL) and 0.05M HCl (50 mL), the organic phase is washed with brine (50 mL) and dried over MgSO4, and the volatile components are evaporated in vacuo. The residue is purified by flash chromatography to give the product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258360B1
Source datasetuspto-grants-2001_07
ORD IDord-8d2444cf38734179abc783926e174926
Source noteuspto-grants-2001_07