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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334554Generated: October 31, 2026

Tetrabutylammonium Fluoride → 1-Fluoro-4-(hexa-1,5-diynyl)benzene

https://huagongshe.com/reaction/334554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(6-(4-Fluorophenyl)hexa-1,5-diynyl)trimethylsilaneHCID 66597810—
SolventTetrahydrofuranHCID 8028—
Product1-Fluoro-4-(hexa-1,5-diynyl)benzeneHCID 8608679145%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (6-(4-fluorophenyl)hexa-1,5-diynyl)trimethylsilane (1.90 g, 7.7 mmol) in THF (24 mL) cooled in a ice bath at 0° C., was added dropwise 7.7 mL of tetrabutylammonium fluoride 1M in THF solution (7.70 mmol). The reaction mixture was stirred 15 min at 0° C., and warmed to room temperature for 2 h 30. The reaction was quenched with water and the aqueous layer was extracted with diethyl ether. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated. The product was purified by flash chromatography (prepacked 25 g silicagel column, DCM 100% as eluent) to afford 500 mg of 1-fluoro-4-(hexa-1,5-diynyl)benzene (Yield: 45%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-031d858e3f104a2a84f847ae8ec1455b
Source noteuspto-grants-2014_11