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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654762Generated: November 2, 2026

Tetrabutylammonium Fluoride → alpha-Ethynylbenzenemethanol

https://huagongshe.com/reaction/1654762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant1-Phenyl-3-(trimethylsilyl)-2-propyn-1-olHCID 2760416—
SolventTetrahydrofuranHCID 8028—
Productalpha-EthynylbenzenemethanolHCID 2015581.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Place a mixture of α-[(trimethylsilyl)ethynyl]-benzenemethanol (4.09 g, 20 mmol) and tetrahydrofuran (25 mL) under argon atmosphere and cool to 0° C. Add, by dropwise addition, tetra-n-butylammonium fluoride (25 mL of a 1M solution in tetrahydrofuran, 25 mmol). Allow to warm to room temperature and stir for 1 hour. Partition between ethyl ether and water. Separate the organic phase, wash with saturated aqueous sodium chloride and concentrate in vacuo. Purify by silica gel chromatography (15% ethyl acetate/hexane) then purify further by distillation to yield 2.15 g of the title compound; bp 100°-110° C. @ 0.1 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05409942
Source datasetuspto-grants-1995_04
ORD IDord-a74e96cfc2e14a7e81c86020571f6f4a
Source noteuspto-grants-1995_04