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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969351Generated: October 31, 2026

2-Hydroxyquinoline → HCID 19379726, compound

https://huagongshe.com/reaction/969351

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-HydroxyquinolineHCID 6038—
ReactantDimethylformamideHCID 6228—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
SolventEthyl AcetateHCID 8857—
ProductHCID 19379726HCID 1937972641%

Reaction Steps

A 7 mL vial was charged with 1H-quinolin-2-one (0.62 g, 4.2 mmol), 4 mL dry DMF and NaH (60% in oil, 0.200 g, 5.1 mmol). The mixture was stirred under a N2 atmosphere at rt for 45 min, and thereafter 1-bromo-3-chloropropane (0.42 mL, 4.2 mmol) was added and the reaction was stirred at rt overnight. The reaction was diluted with EtOAc (50 mL) and washed with water (15 mL). The water phase was extracted with EtOAc (25 mL) and the combined organic phase was dried (Na2SO4), filtered, concentrated under reduced pressure and the residue was purified by flash chromatography (SiO2; CH2Cl2) to yield the title compound (0.38 g, 41%), containing 15% of 1-(3-bromopropyl)-1H-quinolin-2-one. 1H NMR (CD3OD) δ 7.90 (d, J=9.4 Hz, 1H), 7.73-7.57 (m, 3H), 7.34-7.28 (m, 1H), 6.66 (d, J=9.4 Hz), 4.46 (t, J=7.4 Hz, 2H), 3.71 (t, J=6.4 Hz, 2H), 2.21-2.02 (m, 2H); 13C NMR (CD3OD) δ 163.2, 140.7, 138.8, 131.3, 129.3, 122.8, 121.4, 120.2, 114.4, 42.18, 40.2, 30.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307075B2
Source datasetuspto-grants-2007_12
ORD IDord-60fc87f8b64d45b990b2a01ed3995111
Source noteuspto-grants-2007_12