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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380141Generated: October 30, 2026

Water → 1-[8-(Benzyloxy)quinolin-5-yl]ethan-1-one

https://huagongshe.com/reaction/1380141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(8-Hydroxyquinolin-5-yl)ethan-1-one--hydrogen chloride (1/1)HCID 20026880—
SolventDimethylformamideHCID 6228—
Product1-[8-(Benzyloxy)quinolin-5-yl]ethan-1-oneHCID 1374489157.1%

Reaction Steps

27 g of 5-acetyl-8-hydroxyquinoline hydrochloride are dissolved in 540 ml of anhydrous dimethylformamide and 50 g of powdered potassium carbonate are added thereto. 18.4 g of benzyl chloride are added to the mixture at 50° C. under an argon atmosphere, and the mixture is stirred at the same temperature for 4.5 hours and then further stirred at room temperature for 1.5 hours. After the reaction, water is added to the mixture, and the aqueous mixture is extracted with ethyl acetate. The extract is washed with water, a saturated sodium chloride solution, dried and then evaporated under reduced pressure to remove ethyl acetate. The residue is recrystallized from ethanol. 19.1 g of 5-acetyl-8-benzyloxyquinoline are obtained as brownish prisms. 6.35 g of said product are further recovered from the mother liquor.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579854
Source datasetuspto-grants-1986_04
ORD IDord-99211616f59f4803bbd98015a4ae2dfd
Source noteuspto-grants-1986_04