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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190387Generated: October 30, 2026

Potassium Carbonate → HCID 67312595, compound

https://huagongshe.com/reaction/2190387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
Reactant3-(1-cyano-1-methylethyl)-N-(5-hydroxy-2-methylphenyl)benzamideHCID 67312027—
SolventDimethylformamideHCID 6228—
ProductHCID 67312595HCID 6731259570%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1,2-difluoro-4-nitrobenzene (1.19 g, 7.49 mmol) and 3-(1-cyano-1-methylethyl)-N-(5-hydroxy-2-methylphenyl)benzamide (2.0 g, 7.13 mmol) in N,N-dimethylformamide (15 mL) was added potassium carbonate (1.47 g, 10.7 mmol), and the mixture was stirred at 80° C. for 18 hr. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure. The obtained residue was diluted with ethyl acetate (200 mL), washed with water (200 mL) and saturated brine (200 mL), successively, and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=95/5→0/30), and the obtained solution was concentrated under reduced pressure to give the title compound (2.09 g, 70%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324395B2
Source datasetuspto-grants-2012_12
ORD IDord-dd197970bb9a46768ba55ff126ddd73b
Source noteuspto-grants-2012_12