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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201410Generated: October 29, 2026

Dimethylformamide → Methyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoate

https://huagongshe.com/reaction/2201410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-Methoxycarbonylphenylboronic acidHCID 2734369—
Reactant2-Chloro-6-methoxy-3-methylquinolineHCID 4914664—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
ProductMethyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoateHCID 6698005525%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of 2-chloro-6-methoxy-3-methylquinoline (100 mg, 0.482 mmol), 4-(methoxycarbonyl)phenylboronic acid (184 mg, 1.02 mmol), TEA (0.35 mL, 2.41 mmol), and PdCl2(dppf) (35 mg, 0.048 mmol) was added 2 mL of DMF under argon. The mixture was then stirred for 2.5 h at 120° C. in a microwave reactor. The crude mixture was then diluted with water (25 mL) and extracted with EtOAc (25 mL×2). The organics were washed with brine (50 mL), dried over sodium sulfate, and concentrated to yield 250 mg of crude material. The crude was purified via column chromatography with a gradient of 5% EtOAc in hexanes to 80% EtOAc in hexanes to yield 37 mg (25% yield) of methyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364481B2
Source datasetuspto-grants-2016_06
ORD IDord-a041e7ab36e140299c60515b3cb19342
Source noteuspto-grants-2016_06