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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361387Generated: October 29, 2026

Sodium Chloride → 5-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-one

https://huagongshe.com/reaction/1361387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Acetyl-8-hydroxy-2(1H)-quinolinoneHCID 11983895—
SolventDimethylformamideHCID 6228—
Product5-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-oneHCID 1337544480.6%

Reaction Steps

To the product of step (b) (37.7 g, 186 mmol) was added N,N-dimethylformamide (200 mL) and potassium carbonate (34.5 g, 250 mmol) followed by benzyl bromide (31.8 g, 186 mmol). The mixture was stirred at room temperature for 2.25 hour and then poured into saturated sodium chloride (3.5 L) at 0° C. and stirred for 1 hour. The product was collected and dried on a Buchner funnel for 1 hour, and the resulting solids were dissolved in dichloromethane (2 L) and this mixture was dried over sodium sulfate. The solution was filtered through a pad of Celite which was then washed with dichloromethane (5×200 mL). The combined filtrate was then concentrated to dryness and the resulting solids were triturated with ether (500 mL) for 2 h. The product was collected on a Buchner funnel, washed with ether (2×250 mL) and dried under reduced pressure to give 5-acetyl-8-benzyloxy-1H-quinolin-2-one (44 g) as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879879B2
Source datasetuspto-grants-2011_02
ORD IDord-ded9771c707149a281483e55abf16cb2
Source noteuspto-grants-2011_02