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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501986Generated: November 4, 2026

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

https://huagongshe.com/reaction/1501986

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 numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-5e2f7dd6699e4d5292381229b03c7cc4
Source noteuspto-grants-2015_12