Fluorination of α-bromomethyl aryl ketones with fluorohydrogenate-based ionic liquids
-
Add time:07/29/2019 Source:sciencedirect.com
Fluorination of α-bromomethyl aryl ketones using fluorohydrogenate-based ionic liquids as fluorinating reagent is described. Reaction of various α-bromomethyl aryl ketones (1a-g) with fluorohydrogenate-based ionic liquids such as EMIMF·(HF)2.3, PYR13F·(HF)2.3 or PYR14F·(HF)2.3 as a fluoride ion source in anhydrous THF led to the formation of the corresponding α-fluoromethyl aryl ketones (2a–g) in very good yield. Compared to alternative fluorinating agents for this reaction, fluorohydrogenate-based ionic liquids are safer to handle and have the potential to be less expensive and more selective.
We also recommend Trading Suppliers and Manufacturers of -bis(broMoMethyl)- (cas 134457-15-1). Pls Click Website Link as below: cas 134457-15-1 suppliers
Prev:Reduction of 4-(bromomethyl)-2-oxo-2H-chromen-7-yl acetate at carbon cathodes in dimethylformamide and acetonitrile: Lifetime of the electrogenerated radical–anion
Next:Sensitive determination of fluoride in biological samples by gas chromatography–mass spectrometry after derivatization with 2-(bromomethyl)naphthalene) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Cascade regio- and stereoselective reactions of 2-bromomethyl-1,3-thiaselenole with water and ethylene glycol: En roote to the first representatives of polyfunctional 2,3-dihydro-1,4-thiaselenines07/31/2019
- Sensitive determination of fluoride in biological samples by gas chromatography–mass spectrometry after derivatization with 2-(bromomethyl)naphthalene07/30/2019


