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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662540Generated: October 30, 2026

Potassium Carbonate → HCID 57705786, compound

https://huagongshe.com/reaction/1662540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2,5-Difluorophenyl)boronic acidHCID 2734335—
ReactantMethyl 3-(5,5-dimethylcyclopent-1-enyl)-4-(trifluoromethylsulfonyloxy)benzoateHCID 57467618—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 57705786HCID 5770578693%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of methyl 3-(5,5-dimethylcyclopent-1-enyl)-4-(trifluoromethylsulfonyloxy)benzoate 66.6I (0.50 g, 1 mmol) in DMF (7 mL) at 23° C. was added 2,5-difluorophenylboronic acid (0.3 g, 2 mmol, commercially available from Aldrich), and potassium carbonate (0.5 g, 4 mmol). Tetrakis(triphenylphosphine)palladium (0.2 g, 0.1 mmol) was then added to the mixture. The mixture was heated to 90° C. and the reaction was further stirred for 23 hours. The reaction was then cooled to room temperature, diluted with brine and extracted three times with EtOAc. After drying over anhydrous magnesium sulfate and filtering, the organic solvent was removed under reduced pressure and the product was purified on silica gel (0-10% EtOAc in hexanes) to yield 83.25A as a colorless oil (0.42 g, 93% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-2faad86d698d4f72b1fbdec2df3a4fa6
Source noteuspto-grants-2011_10