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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444664Generated: October 31, 2026

Potassium Hydroxide → 1-amino-4-hydroxyquinolin-2(1H)-one

https://huagongshe.com/reaction/1444664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 4-hydroxy-2-oxo-1-{[phenylmethylene]amino}-1,2-dihydroquinoline-3-carboxylateHCID 67063863—
Solvent1,4-DioxaneHCID 31275—
Product1-amino-4-hydroxyquinolin-2(1H)-oneHCID 5916880791%

Reaction Steps

To a solution of 25% by weight aqueous potassium hydroxide (200 mL) and 1,4-dioxane (50 mL) heated to 90-100° C. was added portion wise ethyl 4-hydroxy-2-oxo-1-{[phenylmethylene]amino}-1,2-dihydroquinoline-3-carboxylate (6.72 g, 20.0 mmol). The reaction mixture was heated at reflux for 90 minutes allowing distillation to occur and additional water and dioxane (30 mL each) were added to the reaction vessel to reach the original volume. The mixture was refluxed for an additional 90 minutes with distillation, cooled, washed with 200 mL of 1:1 diethyl ether/ethyl acetate, acidified with concentrated hydrochloric acid to pH 2 and the resulting solid was collected by filtration, washed with water and dried to constant mass to give 1-amino-4-hydroxyquinolin-2(1H)-one as a tan sold (3.22 g, 91% yield), MS (DCI) m/z 177 (M+H)+. 1H NMR (300 MHz, DMSO-d6) δ 5.56 (s, 2H) 5.94 (s, 1H) 7.20 (t, J=7.54 Hz, 1H) 7.62 (m, 1H) 7.85 (m, 2H) 11.33 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662958B2
Source datasetuspto-grants-2010_02
ORD IDord-91069141cd1e4da8aae2b9ec128d86ed
Source noteuspto-grants-2010_02