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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259868Generated: October 27, 2026

Sodium Chloride → 6-Cyano-2-phenyl-4-quinolinecarboxylic acid methyl ester

https://huagongshe.com/reaction/1259868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantDimethylformamideHCID 6228—
ReactantMethyl 6-bromo-2-phenylquinoline-4-carboxylateHCID 4066917—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product6-Cyano-2-phenyl-4-quinolinecarboxylic acid methyl esterHCID 67204437—

Reaction Conditions

Temperature150 °C

Reaction Steps

Zinc cyanide (0.3394 g, 2.89 mmol) and tetrakis(triphenylphosphine)palladium (0.1647 g, 0.143 mmol) were added to a dimethylformamide (14.0 mL) solution of 6-bromo-2-phenyl-4-quinolinecarboxylic acid methyl ester (0.9749 g, 2.85 mmol), and the mixture was heated with stirring at 150° C. for 10 minutes with microwave irradiation. To the reaction solution, water and a saturated aqueous solution of sodium chloride were added. The mixture was subjected to extraction with ethyl acetate and dried over anhydrous sodium sulfate, and then, the solvent was distilled off. The obtained residue was purified by silica gel column chromatography, and the solvent was distilled off to obtain 6-cyano-2-phenyl-4-quinolinecarboxylic acid methyl ester (0.6614 g, 2.29 mmol) as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466290B2
Source datasetuspto-grants-2013_06
ORD IDord-aed87ff42e3543caafecfc90ba252cdf
Source noteuspto-grants-2013_06