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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207973Generated: October 30, 2026

Butane → HCID 118431887, compound

https://huagongshe.com/reaction/2207973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButaneHCID 7843—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 118432096HCID 118432096—
ReactantHCID 131735963HCID 131735963—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 118431887HCID 11843188725.2%

Reaction Conditions

Temperature88 °C

Reaction Steps

To 1-bromo-2,5-difluoro-4-(methylsulfonyl)benzene (19.0 mg, 0.07 mmol), were added 1,2-dimethylethane (1.5 mL) and Pd(PPh3)4 (8.1 mg, cat.). To the reaction mixture, were added 1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-5-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4,5-dihydro-1H-pyrazole (35 mg, 0.07 mmol) prepared in Step 1, ethanol (350.0 uL), and a 2N sodium carbonate solution (350.0 uL). The reaction mixture was stirred at 88° C. for 2 hours. Distilled water was added to the reaction mixture, which was then extracted with diethyl ether two times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a yellow liquid residue. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/5) to give 10.0 mg of the titled compound as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-564af7d37ed14fac8325fd0cf10ae4fa
Source noteuspto-grants-2016_06