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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362781Generated: October 30, 2026

Tetrahydrofuran → Methyl (2'-fluoro[1,1'-biphenyl]-4-yl)acetate

https://huagongshe.com/reaction/1362781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 2-(4-bromophenyl)acetateHCID 316783—
Reactant2-Fluorophenylboronic acidHCID 2734354—
SolventWaterHCID 962—
ProductMethyl (2'-fluoro[1,1'-biphenyl]-4-yl)acetateHCID 12094240—

Reaction Steps

47.6 g (0.21 mol) of methyl 4-bromophenylacetate are introduced under argon into 400 ml of absolute tetrahydrofuran and, at room temperature, 320 ml of 1M sodium carbonate solution and 40 g (0.28 mol) of 2-fluorophenylboronic acid are added. Addition of 7.0 g (0.01 mol) of bis(triphenylphosphane)palladium(II) chloride is followed by heating under reflux for 18 h. Cooling is followed by dilution with 500 ml of water and extracted three times with 300 ml of ethyl acetate each time. The combined organic phases are washed with 400 ml each of saturated ammonium chloride solution, water and saturated sodium chloride solution, dried over magnesium sulfate and freed of solvent in vacuo. Example V is obtained after silica gel filtration (petroleum ether/ethyl acetate 10:1) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07883713B2
Source datasetuspto-grants-2011_02
ORD IDord-d0226dd4d3544808a278e6edf9d8e5c6
Source noteuspto-grants-2011_02