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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926126Generated: November 2, 2026

Water → 4-((Tert-butyldimethylsilyl)oxy)but-2-yn-1-ol

https://huagongshe.com/reaction/1926126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Butyne-1,4-diolHCID 8066—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventTetrahydrofuranHCID 8028—
Product4-((Tert-butyldimethylsilyl)oxy)but-2-yn-1-olHCID 546184521.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

60% Sodium hydride (1.39 g) was suspended in tetrahydrofuran (50 mL), and the suspension was cooled to 0° C., a solution of but-2-yne-1,4-diol (3.0 g) in tetrahydrofuran (20 mL) was added dropwise, and the mixture was stirred at room temperature for 1 hr. tert-Butyldimethylsilyl chloride (5.26 g) was added to the reaction mixture, and the mixture was stirred at room temperature for 24 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=100:0→80:20) to give the title compound (1.48 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-f792aa72cc5f40bd8f688cc0b71cab93
Source noteuspto-grants-2012_05