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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044765Generated: October 30, 2026

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

https://huagongshe.com/reaction/2044765

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

At first, 75.0 g of 4-bromo-3-fluorophenol (S3-1), 82.9 g of 3,4,5-trifluorophenyl-boric 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, and the mixture was heated to 80° C. and stirred for 4 hr. Next, the reaction solution was cooled to room temperature, added with toluene and then washed with 1N hydrochloric acid and water. Afterwards, the solution was dried over magnesium sulfate and distilled under reduced pressure to remove the solvent. Subsequently, the product was purified by silica-gel column chromatography with a mixed solvent of heptane/ethyl acetate=4/1 as the 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 (S3-3) from (S3-1) was 81.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586803B2
Source datasetuspto-grants-2013_11
ORD IDord-f756be29c2214a45949dfd1698a182ee
Source noteuspto-grants-2013_11