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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422282Generated: October 30, 2026

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

https://huagongshe.com/reaction/422282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(6-(4-Fluorophenyl)hexa-1,5-diynyl)trimethylsilaneHCID 66597810—
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 TH F (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 numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-2ecf01d8633544d8b98811103d102f56
Source noteuspto-grants-2012_01