Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191340Generated: October 31, 2026

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

https://huagongshe.com/reaction/1191340

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 numberUS08680115B2
Source datasetuspto-grants-2014_03
ORD IDord-c4a794c1289d4602a814bba217af5bcc
Source noteuspto-grants-2014_03