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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207961Generated: November 1, 2026

Ethanol → HCID 118432017, compound

https://huagongshe.com/reaction/2207961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant3-Acetylphenylboronic acidHCID 2734310—
ReactantHCID 118431784HCID 118431784—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 118432017HCID 11843201720.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-(3-Bromo-pyridin-6-yl)-1-(2-chloro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (20.0 mg, 0.04 mmol) prepared in Step 4 of Preparation 3, 3-acetylphenylboronic acid (11.0 mg, 0.07 mmol), Pd(PPh3)4 (2.0 mg, cat.) and a 2N sodium carbonate solution (210.0 uL) were added to a mixed solvent of ethanol (210.0 uL) and toluene (310.0 uL). The reaction mixture was stirred at 80° C. for 1 hour and then filtered through celite pad. A saturated solution of ammonium chloride was added to the filtrate, which was then extracted with ethyl acetate three 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=1/6) to give 4.0 mg of the titled compound as a white liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-86566233b8c64fd2afceb28dfcae8beb
Source noteuspto-grants-2016_06