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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3116Erstellt: 23. Oktober 2026

Water → Dimethyl 7-chloroquinoline-2,3-dicarboxylate

https://huagongshe.com/de/reaction/3116

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium FormateHCID 2723810—
EduktDimethyl 4,7-dichloroquinoline-2,3-dicarboxylateHCID 18929951—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelDimethylformamideHCID 6228—
ProduktDimethyl 7-chloroquinoline-2,3-dicarboxylateHCID 18929843134,8%

Reaktionsschritte

A stirred mixture of dimethyl 4,7-dichloroquinoline-2,3-dicarboxylate (5.00 g, 15.9 mM), sodium formate (1.63 g, 23.9 mM) and tetrakis(triphenylphosphine)palladium(0) (0.92 g, 0.80 mM) in anhydrous dimethylformamide (75 mL) under a nitrogen atmosphere was heated at 90°-95° C. for 7 hr. No reaction occurred so the reaction mixture was degassed and an additional quantity of tetrakis(triphenylphosphine)palladium(0) (0.92 g, 0.80 mM) was added and the reaction mixture again heated at 90°-95° C. for 6 hr. The cooled reaction mixture was poured into water and the resulting mixture extracted with ethyl acetate. The combined extracts were dried (MgSO4), filtered and concentrated to leave an gummy solid (6.0 g). Trituration of this residue with ethyl acetate and subsequent filtration separated a crystalline solid which was shown to be dimethyl 7-chloro-4-hydroxyquinoline-2,3-dicarboxylate. The filtrate was concentrated and the residue was flash chromatographed over silica gel (eluant: hexane/ethyl acetate, 3/2) to provide the title diester (1.13 g, 25.4%) as a light yellow crystalline solid; MS(CI): 280 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05733910
Quelldatensatzuspto-grants-1998_03
ORD IDord-e1f559619b474a8e8ddc858df147e65a
Quellennotizuspto-grants-1998_03