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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771817Generated: October 30, 2026

Dimethylformamide → 5-(3,4-Difluorophenyl)-2,3-dimethyl-benzoic acid

https://huagongshe.com/reaction/1771817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium CarbonateHCID 10340—
Reactant3,4-Difluorobenzeneboronic acidHCID 2734337—
Reactant5-Bromo-2,3-dimethylbenzoic acidHCID 66895989—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-(3,4-Difluorophenyl)-2,3-dimethyl-benzoic acidHCID 8944528470%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 5-bromo-2,3-dimethyl-benzoic acid (500 mg, 2.18 mmol, 1.0 eq), (3,4-difluorophenyl)boronic acid (378.6 mg, 2.40 mmol, 1.1 eq) and Na2CO3 (693 mg, 6.54 mmol, 3.0 eq) in a mixture of EtOH (2.5 mL), DMF (10 mL) and H2O (2.5 mL) was added Pd(PPh3)4 (126 mg, 0.11 mmol, 0.05 eq) under nitrogen. The mixture was stirred at 100° C. overnight. After cooling to room temperature, water was added and the diluted reaction mixture filtered through celite. The aqueous layer was extracted with EtOAc and the organic extract was discarded. The remaining aqueous layer was acidified to pH 2 by addition of 3M HCl. The resulting mixture was extracted with EtOAc and the combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo to give the title compound as a white solid (400 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249085B2
Source datasetuspto-grants-2016_02
ORD IDord-3415f8a2e6b6415c8fabd44d6304c278
Source noteuspto-grants-2016_02