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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332638Generated: October 30, 2026

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

https://huagongshe.com/reaction/332638

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 numberUS08877774B2
Source datasetuspto-grants-2014_11
ORD IDord-7f5f73ac0f58484d8c90f3d9d86f6a45
Source noteuspto-grants-2014_11