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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239198Generated: November 1, 2026

Sodium Carbonate → 2,3',4',5'-Tetrafluorobiphenyl-4-ol

https://huagongshe.com/reaction/2239198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-3-fluorophenolHCID 2779153—
ReactantWater 1,2-dimethoxyethaneHCID 18180031—
ReactantHCID 21870694HCID 21870694—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2,3',4',5'-Tetrafluorobiphenyl-4-olHCID 2105214481.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

Firstly, 75.0 g of 4-bromo-3-fluorophenol (S3-1), 82.9 g of 3,4,5-trifluoro-phenylboric acid (S3-2), 13.6 g of tetrakis(triphenylphosphine)palladium, 108.5 g of sodium carbonate and 1100 ml of a mixed solvent of dimethoxyethane/water=2/1 (volume ratio) were added into a reactor under nitrogen atmosphere, heated to 80° C., and stirred for 4 hours. Next, the reaction solution was cooled to room temperature, added with toluene, and then washed with 1N HCl(aq) and water. Afterwards, the solution was dried with magnesium sulphate, and distilled under reduced pressure to remove the solvent. Subsequently, the product was purified by silica-gel column chromatography with heptane/ethyl acetate (4/1) as an eluent, and then dried under reduced pressure. The obtained residue was recrystallized in heptane, to obtain 77.5 g of 3-fluoro-4-(3,4,5-trifluorophenyl)phenol (S3-3). The yield of compound (S3-3) from (S3-1) was 81.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07722783B2
Source datasetuspto-grants-2010_05
ORD IDord-fa252bcab4994fc8a691ab0ce5a151eb
Source noteuspto-grants-2010_05