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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986499Generated: October 31, 2026

Dimethylformamide → HCID 51050345, compound

https://huagongshe.com/reaction/1986499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAcroleinHCID 7847—
ReactantTriethylamineHCID 8471—
ReactantHCID 51050239HCID 51050239—
CatalystBenzyl triethylammonium chlorideHCID 66133—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
ProductHCID 51050345HCID 5105034570%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 6-bromo-2-isobutyl-4-(4-methylphenyl)quinoline-3-carbonitrile (5.00 g, 13.2 mmol), acrolein (2.22 g, 39.6 mmol), benzyltriethylammonium chloride (3.00 g, 13.2 mmol), triethylamine (5.5 ml, 39.6 mmol), palladium acetate (150 mg, 0.66 mmol) and N,N-dimethylformamide (40 ml) was stirred under an argon atmosphere at 70° C. After 3 hrs., palladium acetate (150 mg, 0.66 mmol) and acrolein (2.22 g, 39.6 mmol) were added to the reaction mixture and the mixture was stirred at the same temperature for 17 hrs. The reaction mixture was diluted with ethyl acetate, washed 4 times with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography to give 2-isobutyl-4-(4-methylphenyl)-6-[(1E)-3-oxoprop-1-en-1-yl]quinoline-3-carbonitrile (3.26 g, yield 70%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547710B2
Source datasetuspto-grants-2009_06
ORD IDord-0b779852038d4c57818a023700003de4
Source noteuspto-grants-2009_06