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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181322Generated: October 26, 2026

Iodine → Bis(3-fluorophenyl)methanol

https://huagongshe.com/reaction/1181322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthyl formateHCID 8025—
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductBis(3-fluorophenyl)methanolHCID 275825099.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of magnesium strip (35.4 g) in THF (200 ml), iodine strip was added and the mixture was heated with stirring under nitrogen stream until most of color of iodine was disappeared. A solution of 3-fluoro-bromobenzene (250.0 g) in THF (1000 ml) was added dropwise over 2.5 hr while the temperature of the solution was maintained at 60° C., After the completion of the addition of the solution, the resulting mixture was refluxed for 1 hr with heating. The resulting Grignard solution was ice-cooled and a solution of ethyl formate (63.2 g) in THF (200 ml) was added dropwise over 1 hr. After a stirring of the reaction solution for an additional 30 min, saturated aqueous ammonium chloride solution (700 ml) was added dropwise with ice-cooling and water (300 ml) was added. The mixture was stirred for 10 min. The organic layer and water layer were separated. Water layer was extracted with ethyl acetate, and the combined organic layer was washed with 2N hydrochloric acid, saturated aqueous sodium hydrogencarbonate and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and the solvent was evaporated off under reduced pressure to give the title compound (156.2 g, yield 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285551B2
Source datasetuspto-grants-2007_10
ORD IDord-88121eea85004e9c9873ebf7bd1efab4
Source noteuspto-grants-2007_10