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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918628Generated: October 26, 2026

Pyridine → 4-(Triethylsilyl)but-3-yn-1-yl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/1918628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-(Triethylsilyl)-3-butyn-1-olHCID 2760694—
SolventDichloromethaneHCID 6344—
Product4-(Triethylsilyl)but-3-yn-1-yl 4-methylbenzene-1-sulfonateHCID 12030138102.5%

Reaction Steps

A solution of 4-(triethylsilyl)but-3-yn-1-ol (2 mL; 9.22 mmol), p-toluensulfonyl chloride (3.52 g; 18.44 mmol) and pyridine (1.49 mL; 18.44 mmol) in dichloromethane (30 mL) was stirred at room temperature for 3 days. The reaction mixture was then washed with a saturated solution of sodium hydrogen sulphate and brine. The organic layer was dried, concentrated under reduced pressure and the crude material was purified by flash chromatography on silica gel (eluent 2 to 20% ethyl acetate in heptane) to yield 3.20 g (quantitative yield) of 4-(triethylsilyl)but-3-ynyl 4-methylbenzenesulfonate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-cf4519f69f8141f7bf2cf1403b8f4875
Source noteuspto-grants-2013_12