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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 628850Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/628850

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt4-Methoxycarbonylphenylboronic acidHCID 2734369—
Edukt2-Chloro-6-methoxy-3-methylquinolineHCID 4914664—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelWaterHCID 962—
ProduktMethyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoateHCID 6698005525%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09315462B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-972b8b97ff7b4039b1d08ea32c45a9ac
Quellennotizuspto-grants-2016_04