HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228908Generated: October 29, 2026
2'-Hydroxy-4',5'-dimethylacetophenone → HCID 57756422, compound
https://huagongshe.com/reaction/228908
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2'-Hydroxy-4',5'-dimethylacetophenone | HCID 118976 | — |
| Reactant | 7-(Benzyloxy)-4-chloro-6-methoxyquinoline | HCID 22646562 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | HCID 57756422 | HCID 57756422 | 51.4% |
Reaction Steps
2-Hydroxy-4,5-dimethylacetophenone (3.63 g), 7-benzyloxy-4-chloro-6-methoxyquinoline (1.50 g), and 4-dimethylaminopyridine (2.71 g) were suspended in o-dichlorobenzene (15 ml), and the suspension was stirred at 130° C. overnight. The reaction solution was cooled to room temperature, and the solvent was then removed by distillation under the reduced pressure. Water was added to the residue, and the mixture was extracted with chloroform, and the chloroform layer was then washed with water and saturated brine and was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-hexane to give the title compound (1.10 g, yield 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-859197e649ea4668a1137e8974515726 |
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| Source note | uspto-grants-2009_07 |
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