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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986676Generated: November 3, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 6-Fluoro-1,2-dihydroquinolin-2-one

https://huagongshe.com/reaction/1986676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant6-Fluoro-3,4-dihydroquinolin-2(1H)-oneHCID 13690765—
Solvent1,4-DioxaneHCID 31275—
Product6-Fluoro-1,2-dihydroquinolin-2-oneHCID 983404331.2%

Reaction Steps

DDQ (0.38 g, 1.7 mmol) was added to a solution of 6-fluoro-3,4-dihydro-1H-quinolin-2-one (0.18 g, 1.1 mmol) in dioxane (25 mL) and the resulting solution was refluxed for 16 h. The mixture was concentrated, and sat aqueous Na2CO3 (25 mL) was added followed by extraction into an organic mixture (MeOH:CH2Cl2; 1:10, 3×50 mL). The combined organic phase was dried (Na2SO4), filtered, concentrated under reduced pressure and purified by flash CC (SiO2; CH2Cl2/MeOH 20:1) to give the title compound (0.056 g, 31%). 1H NMR (DMSO-D6) δ 11.8 (brs, 1H), 7.85 (d, J=9.4 Hz), 7.50 (dd, J=2.8, 9.2 Hz), 7.43-7.37 (m, 1H), 7.37-7.25 (m, 1H), 6.54 (d, J=9.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550459B2
Source datasetuspto-grants-2009_06
ORD IDord-2617f7da3a174204adef1f046d377337
Source noteuspto-grants-2009_06