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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905561Generated: October 30, 2026

Diethyl Malonate → HCID 66885525, compound

https://huagongshe.com/reaction/905561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
ReactantSodium BisulfateHCID 516919—
Reactant4-Bromo-3-chloro-6-fluoroquinolineHCID 45925762—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 66885525HCID 66885525113.3%

Reaction Steps

To a suspension of NaH (60% in oil dispersion, 2.2 g, 54 mmol) in 1,4-dioxane (26 mL) was added diethyl malonate (9 mL, 59 mmol). The reaction mixture was stirred at rt for 5 min and heated at 80° C. for 1 h. After cooling to rt, CuBr (1.0 g) and 4-bromo-3-chloro-6-fluoro-quinoline (5 g, 19.4 mmol) in dioxane (8 mL) were successively added. The mixture was stirred at 100° C. overnight. After cooling, 10% aq. NaHSO4 (100 mL) was added. The mixture was stirred 30 min. The two layers were decanted and the aq. layer was extracted three times with EA (3×150 mL). The combined org. layers were washed with brine, dried over Na2SO4, filtered and concentrated to dryness. The residue was triturated in DCM to yield the title compound as a yellow solid (6.71 g, 100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012961B2
Source datasetuspto-grants-2011_09
ORD IDord-16049609f29343fa9738c7ddcf09f9b0
Source noteuspto-grants-2011_09