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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771645Generated: November 1, 2026

Water → 4-Chloro-3'-fluoro-[1,1'-biphenyl]-3-carboxylic acid

https://huagongshe.com/reaction/1771645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-2-chlorobenzoic acidHCID 33127—
Reactant3-Fluorophenylboronic acidHCID 2733986—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Product4-Chloro-3'-fluoro-[1,1'-biphenyl]-3-carboxylic acidHCID 4631447567%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 3-fluorophenyl boronic acid (500 mg, 3.5 mmol, 1.2 eq), 5-bromo-2-chlorobenzoic acid (700 mg, 3.0 mmol, 1.0 eq), Pd(PPh3)4 (687 mg, 0.60 mmol, 0.2 eq) and Na2CO3 (2.52 g, 24 mmol, 8.0 eq) in a mixture of ethanol (5 mL), H2O (5 mL) and DMF (20 mL) was stirred at 100° C. under N2 overnight. The reaction was quenched by addition of diluted HCl (to pH 3) and the aqueous phase was extracted with EtOAc. The combined organic extracts were washed with brine, dried (Na2SO4) filtered and evaporated in vacuo. The residue was purified by chromatography (petroleum ether:EtOAc 20:1 to 1:1) to give the title compound as a white solid (500 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249085B2
Source datasetuspto-grants-2016_02
ORD IDord-f006e62019f14ad89187242f92796d37
Source noteuspto-grants-2016_02