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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3116Generated: October 25, 2026

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

https://huagongshe.com/reaction/3116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium FormateHCID 2723810—
ReactantDimethyl 4,7-dichloroquinoline-2,3-dicarboxylateHCID 18929951—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductDimethyl 7-chloroquinoline-2,3-dicarboxylateHCID 18929843134.8%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733910
Source datasetuspto-grants-1998_03
ORD IDord-e1f559619b474a8e8ddc858df147e65a
Source noteuspto-grants-1998_03