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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-(2-Amino-4-(benzyloxy)-5-methoxyphenyl)ethanone | HCID 22667147 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(Benzyloxy)-6-methoxyquinolin-4-ol | HCID 22646579 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06797823B1 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-08abb0a7001c42cfa9de11be440039c4 |
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| Source note | uspto-grants-2004_09 |
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