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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392295Generated: October 29, 2026

Potassium Carbonate → methyl 4-(1-ethyl-1H-pyrazol-5-yl)-5-methyl-2-furancarboxylate

https://huagongshe.com/reaction/2392295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-bromo-5-methylfuran-2-carboxylateHCID 604544—
Reactant1-Ethylpyrazole-5-boronic acid, pinacol esterHCID 53217252—
CatalystHCID 178418851HCID 178418851—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
Productmethyl 4-(1-ethyl-1H-pyrazol-5-yl)-5-methyl-2-furancarboxylateHCID 57826453—

Reaction Conditions

Temperature72 °C

Reaction Steps

To a 100 mL sealed flask was added 1-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (2.2 g, 9.91 mmol), potassium carbonate (2.84 g, 20.54 mmol), methyl 4-bromo-5-methyl-2-furancarboxylate (1.5 g, 6.85 mmol) and BIS(TRI-T-BUTYLPHOSPHINE)PALLADIUM(0) (0.175 g, 0.34 mmol) in 1,2-dimethoxyethane (6 mL) and H2O (1 mL). After stirring for 2 h at 72° C., the reaction solution was diluted with DCM (50 mL) and washed with H2O. The organic layer was dried Na2SO4, filtered and concentrated. The residue was purified on silica gel [EtOAC/hexanes, 10-30%] to give the product [1.1 g, 68.6%] as an off white solid: LC-MS (ES) m/z 235 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273782B2
Source datasetuspto-grants-2012_09
ORD IDord-a107ca1d7cd04c83bd56af902ea3beb3
Source noteuspto-grants-2012_09