HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228588Generated: October 27, 2026
Chlorohydroxy benzophenone → {5-Chloro-2-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-(phenyl)methanone
https://huagongshe.com/reaction/228588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorohydroxy benzophenone | HCID 6799 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | {5-Chloro-2-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-(phenyl)methanone | HCID 24879149 | — |
Reaction Steps
4-Chloro-6,7-dimethoxyquinoline (57.5 mg), 5-chloro-2-hydroxybenzophenone (309 mg), and 4-dimethylaminopyridine (173 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 160° C. for 5 hr. The mixture was cooled to room temperature, and the solvent was then removed therefrom by distillation under the reduced pressure, and chloroform was added to the residue. The mixture was washed with a 1 N aqueous potassium hydroxide solution and saturated brine and was dried over anhydrous magnesium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using chloroform and by thin layer chromatography using acetone-hexane to quantitatively give 114 mg of the title compound.
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-8277d72b42fa453baf4ae54bd8eea696 |
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| Source note | uspto-grants-2009_07 |
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