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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517350Generated: November 1, 2026

Toluene → 5-[3-(Methoxycarbonyl)phenyl]furan-2-carboxylic acid

https://huagongshe.com/reaction/517350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant5-Bromo-2-furanecarboxylic acidHCID 68511—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(Methoxycarbonyl)benzeneboronic acidHCID 2734714—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-[3-(Methoxycarbonyl)phenyl]furan-2-carboxylic acidHCID 418954191%

Reaction Conditions

Temperature90 °C

Reaction Steps

To 5-bromofuran-2-carboxylic acid (0.50 g, 2.6 mmol), 3-methoxycarbonylphenylboronic acid (0.52 g, 2.9 mmol), tetrakis(triphenylphosphine)palladium (45 mg, 0.039 mmol), and sodium hydrogen carbonate (0.49 g, 5.9 mmol) were added toluene (3.5 mL), tetrahydrofuran (3.0 mL) and water (3.5 mL), and the mixture was stirred at 90° C. for 2 hours. Water was added to the reaction mixture, and the mixture was washed with ethyl acetate. The aqueous layer was acidified with 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound as a pale-yellow powder (0.58 g, 2.3 mmol, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115107B2
Source datasetuspto-grants-2015_08
ORD IDord-9e503848dbba424ab5b84f8c6e0abb22
Source noteuspto-grants-2015_08