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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205681Generated: November 3, 2026

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

https://huagongshe.com/reaction/2205681

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 (Bu4NBr3) (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%). 1H NMR (400 MHz, DMSO-d6): δ 11.07 (s, 1H); 8.51 (d, J=10.0 Hz, 1H); 7.94-7.83 (m, 1H); 7.60 (d, J=7.5 Hz, 2H); 7.44-7.27 (m, 4H); 6.79-6.65 (m, 1H); 5.53-5.39 (s, 2H); 4.93 (s, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371318B2
Source datasetuspto-grants-2016_06
ORD IDord-076a359b3fa14dd197e44b45833db20c
Source noteuspto-grants-2016_06