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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112744Generated: November 1, 2026

Ammonia → 2-Hydroxyquinolin-8-yl acetate

https://huagongshe.com/reaction/2112744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAcetic AnhydrideHCID 7918—
Reactant8-Hydroxyquinoline N-oxideHCID 14312—
Product2-Hydroxyquinolin-8-yl acetateHCID 268240—

Reaction Steps

Quinolin-8-ol 1-oxide (20 g, 124 mmol) in acetic anhydride (200 ml) was stirred at 90° C. for 5 hours. Then the reaction mixture was poured into water/ice mixture (1.5 L), and made neutral by addition of conc. aq. NH3. The precipitate formed was collected by filtration and washed with water. The crude product was purified by suspending in propan-2-ol and addition of petroleum ether to give 2-oxo-1,2-dihydroquinolin-8-yl acetate. 2-Oxo-1,2-dihydroquinolin-8-yl acetate was heated in conc. aq. HCl (200 ml) at 90° C. for 4 hours. The reaction mixture was poured into ice-cold water (400 ml), and the precipitate formed was collected by filtration and washed with water. Recrystallization from propan-2-ol/petroleum ether afforded the subtitle compound (14.1 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524856B2
Source datasetuspto-grants-2009_04
ORD IDord-a502f6f7cc834615b8ccbcb2240a9129
Source noteuspto-grants-2009_04