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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008322Generated: October 30, 2026

Sulfuric Acid → 7-(Benzyloxy)-6-methoxyquinolin-4-ol

https://huagongshe.com/reaction/1008322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl formateHCID 8025—
ReactantSodium MethoxideHCID 10942334—
Reactant1-(2-Amino-4-(benzyloxy)-5-methoxyphenyl)ethanoneHCID 22667147—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product7-(Benzyloxy)-6-methoxyquinolin-4-olHCID 2264657966%

Reaction Steps

1-[2-Amino-4-(benzyloxy)-5-methoxyphenyl]-1-ethanone (24.95 g) was dissolved in tetrahydrofuran (450 ml), and sodium methoxide (24.87 g) was added to the solution. The mixture was stirred at room temperature for one hr. Ethyl formate (37.07 ml) was then added thereto, and the mixture was stirred at room temperature for 2 hr. Water (150 ml) was then added thereto, and the mixture was stirred overnight. The reaction solution was adjusted to pH 4 by the addition of concentrated sulfuric acid at 0° C. Water was added thereto, and the mixture was extracted with chloroform. The chloroform layer was dried over sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by chromatography on silica gel by development with chloroform/methanol (10/1) to give 17.16 g (yield 66%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797823B1
Source datasetuspto-grants-2004_09
ORD IDord-08abb0a7001c42cfa9de11be440039c4
Source noteuspto-grants-2004_09