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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961275Generated: November 1, 2026

Potassium Carbonate → 5-methyl-4-(1-methyl-1H-pyrazol-5-yl)-2-furancarboxylic acid

https://huagongshe.com/reaction/1961275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-bromo-5-methylfuran-2-carboxylateHCID 604544—
Reactant1-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 4912908—
CatalystHCID 178418851HCID 178418851—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-methyl-4-(1-methyl-1H-pyrazol-5-yl)-2-furancarboxylic acidHCID 5782656485.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 4-bromo-5-methyl-2-furancarboxylate (500 mg, 2.28 mmol), 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (950 mg, 4.57 mmol)[prepared according to Preparation 7] and potassium carbonate (315 mg, 2.28 mmol) in 1,4-dioxane (8 mL) and water (2.0 mL) was added bis(tri-t-butylphosphine)Palladium (0) (117 mg, 0.23 mmol). The mixture was heated to 80° C. and after 15 h the reaction mixture was concentrated. The residue was partitioned between DCM and water. The organic layer was concentrated and dissolved in tetrahydrofuran (THF) (8.0 mL). The solution was treated with 6N aqueous solution of sodium hydroxide (3.80 mL, 22.83 mmol) and heated to 75° C. After 15 h, the reaction mixture was concentrated and partitioned between DCM and water. The aqueous layer was acidified to pH ˜3 with 2N HCl aqueous solution and extracted several times with DCM. The organic fractions were combined and concentrated to afford the title compound as a yellow solid (401 mg, 1.95 mmol, 85% yield): LC-MS (ES) m/z 207 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410158B2
Source datasetuspto-grants-2013_04
ORD IDord-74b81ebb6f364aeda2653792743d6e6f
Source noteuspto-grants-2013_04