Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735086Generated: October 30, 2026

Tetrabutylammonium Fluoride → 1,3,5-Trichloro-2-ethynylbenzene

https://huagongshe.com/reaction/735086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantTriphenyl-(2,4,6-trichlorophenylethynyl)silaneHCID 86060684—
SolventTetrahydrofuranHCID 8028—
Product1,3,5-Trichloro-2-ethynylbenzeneHCID 19378029—

Reaction Steps

A reaction mixture of 5 g (10.8 mmol) of triphenyl-(2,4,6-trichlorophenylethynyl)silane and 4.2 g (16.2 mmol) of tetrabutylammonium fluoride in 50 mL of absolute THF is stirred for half an hour at ambient temperature and then evaporated down. The residue is taken up in diethyl ether and water and extracted. The organic phase is dried over sodium sulfate. The purification is carried out by column chromatography on silica gel (eluant: petroleum ether/toluene (9:1)). Yield: 0.46 g (20.7% of theory); Rf value: 0.6 (silica gel, petroleum ether/toluene (9:1)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592373B2
Source datasetuspto-grants-2009_09
ORD IDord-427c66677cd246d5bb7cf7e5312da80a
Source noteuspto-grants-2009_09