HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905561Generated: October 30, 2026
Diethyl Malonate → HCID 66885525, compound
https://huagongshe.com/reaction/905561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | 4-Bromo-3-chloro-6-fluoroquinoline | HCID 45925762 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 66885525 | HCID 66885525 | 113.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012961B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-16049609f29343fa9738c7ddcf09f9b0 |
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| Source note | uspto-grants-2011_09 |
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