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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674606Generated: November 1, 2026

Triethylamine → 4-{5-[(E)-2-Ethoxycarbonylvinyl]-3-cyanoindol-1-yl}benzoic acid

https://huagongshe.com/reaction/1674606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcrylateHCID 8821—
ReactantTriphenylphosphineHCID 11776—
Reactant4-(5-Bromo-3-cyanoindol-1-yl)benzoic acid ethyl esterHCID 25052346—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-{5-[(E)-2-Ethoxycarbonylvinyl]-3-cyanoindol-1-yl}benzoic acidHCID 6661736135.9%

Reaction Steps

A solution of 4-(5-bromo-3-cyanoindol-1-yl)benzoic acid ethyl ester (0.1 g), acrylic acid ethyl ester (0.11 g) and triethylamine (0.082 g) in N,N-dimethylformamide (2 mL) was stirred in the presence of palladium (II) acetate (0.0061 g) and triphenylphosphine (0.014 g) at 100° C. for 30 hours. This reaction mixture was poured into water, and this resulting mixture was extracted with ethyl acetate twice. This organic layer was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: ethyl acetate/n-hexane=10/90-75/25) to give the title compound (0.035 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003647B2
Source datasetuspto-grants-2011_08
ORD IDord-b2370c7d7a57404584122cb526fbf545
Source noteuspto-grants-2011_08