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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175812Generated: October 31, 2026

Ethanol → 3-Ethenyl-6-fluoro-2-methylbenzonitrile

https://huagongshe.com/reaction/2175812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3-Bromo-6-fluoro-2-methylbenzonitrileHCID 66643852—
CatalystHCID 178418807HCID 178418807—
Product3-Ethenyl-6-fluoro-2-methylbenzonitrileHCID 66643866—

Reaction Steps

3-Bromo-6-fluoro-2-methylbenzonitrile (23.6 g, 110 mmol), potassium vinyl trifluoroborate (29.5 g, 221 mmol), PdCl2(dppf)-CH2Cl2 Adduct (4.03 g, 5.51 mmol), and TEA (30.7 mL, 221 mmol) were added to 250 mL of ethanol. The reaction mixture was degassed then stirred at reflux for 4 h. LC-MS confirmed the presence of product. The reaction mixture was diluted with ethyl acetate, washed twice with brine, dried, and evaporated to dryness. The crude material was then purified by MPLC chromatography using a 330 g Redi-sep column and eluting with a 10% EtOAc/Hexane solvent system to yield 3-ethenyl-6-fluoro-2-methylbenzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062070B2
Source datasetuspto-grants-2015_06
ORD IDord-07f42805eeff41c796d12765556246f3
Source noteuspto-grants-2015_06