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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053753Generated: October 31, 2026

Water → 4-(2,5-Dihydro-1H-pyrrole-1-carbonyl)-3-methylbenzonitrile

https://huagongshe.com/reaction/2053753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant(4-Bromo-2-methylphenyl)(2,5-dihydro-1H-pyrrol-1-yl)methanoneHCID 22600480—
ReactantHCID 178418260HCID 178418260—
SolventDimethylformamideHCID 6228—
Product4-(2,5-Dihydro-1H-pyrrole-1-carbonyl)-3-methylbenzonitrileHCID 22600482—

Reaction Conditions

Temperature140 °C

Reaction Steps

31.6 g (0.11 mol) of 4-(2,5-dihydropyrrol-1-ylcarbonyl)-3-methylbromobenzene is dissolved in 125 mL of dimethylformamide and combined with 20.2 g (0.23 mol) of copper cyanide and 3.2 g (2.7 mmol) of tetrakis-triphenylphosphinepalladium(0). The suspension is stirred for 20 hours at 140° C. Then it is cooled to 80° C., combined with 150 mL of water, 150 mL of ethyl acetate, and 25 g of CELITE® filter aid and filtered through CELITE® filter aid. The organic phase is separated off, washed with sodium chloride solution, dried over sodium sulfate, and concentrated by evaporation. The residue is chromatographed on silica gel, eluting with ethyl acetate/ethanol (50:1 and 19:1). The corresponding fractions are combined and concentrated by evaporation. Yield: 11.7 g (49% of theory); Rf value: 0.55 (silica gel; ethyl acetate/ethanol=9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326791B2
Source datasetuspto-grants-2008_02
ORD IDord-fc94ac9fc4c046f4bf3b57cbbd5699c5
Source noteuspto-grants-2008_02