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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874799Generated: November 3, 2026

5-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-one → 8-Benzyloxy-5-(2-bromoacetyl)-2-hydroxyquinoline

https://huagongshe.com/reaction/874799

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-oneHCID 13375444—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product8-Benzyloxy-5-(2-bromoacetyl)-2-hydroxyquinolineHCID 1166786773%

Reaction Steps

To a suspension of 5-acetyl-8-(benzyloxy)quinolin-2(1H)-one (19.4 g, 66.4 mmol) in anhydrous THF (240 mL) and anhydrous methanol (165 mL) was added a solution of tetra-n-butylammonium tribromide (54.5 g, 113.0 mmol) in anhydrous THF (130 mL) dropwise over 1.5 hours. The resulting solution was stirred at RT overnight before concentrating under reduced pressure without heating. The residue was re-dissolved in methanol (200 mL). Saturated aqueous ammonium chloride solution (390 mL) was added with ice-cooling. The resulting suspension was filtered and the solid washed with water and air-dried under vacuum. The solid was suspended in DCM and methanol (1:1 v/v, 100 mL) for 90 minutes. The solid was collected by filtration, washed with DCM and air-dried to afford the title compound (18.0 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980913B2
Source datasetuspto-grants-2015_03
ORD IDord-557e7eb0a11b4d60bd406672e9b6c22f
Source noteuspto-grants-2015_03