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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845686Generated: October 30, 2026

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

https://huagongshe.com/reaction/1845686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-Bromo-5-chloro-2-furoateHCID 12239445—
Reactant1-Ethylpyrazole-5-boronic acid, pinacol esterHCID 53217252—
CatalystHCID 178418851HCID 178418851—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
Productmethyl 5-chloro-4-(1-ethyl-1H-pyrazol-5-yl)-2-furancarboxylateHCID 5782675650.1%

Reaction Conditions

Temperature75 °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 (2.61 g, 11.74 mmol), potassium carbonate (3.25 g, 23.48 mmol), methyl 4-bromo-5-chloro-2-furancarboxylate (1.85 g, 8.33 mmol) and bis(tri-t-butylphosphine)palladium(0) (0.16 g, 0.31 mmol) in 1,2-Dimethoxyethane (DME) (30 mL) and H2O (5 mL). After stirring for 2 h at 75° C., the reaction solution was diluted with DCM (100 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 (0.8 g, 50.1%) as an off-white solid: LC-MS (ES) m/z 255 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946278B2
Source datasetuspto-grants-2015_02
ORD IDord-e3ad2615ee8a4cd19643d4a697200190
Source noteuspto-grants-2015_02