HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533398Generated: October 27, 2026
Cesium fluoride → Methyl 3-chloro-4-(2,4-difluorophenyl)quinoline-6-carboxylate
https://huagongshe.com/reaction/533398
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2,4-Difluorophenylboric acid | HCID 22237829 | — |
| Reactant | Methyl 4-bromo-3-chloroquinoline-6-carboxylate | HCID 67773454 | — |
| Catalyst | HCID 178506421 | HCID 178506421 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-chloro-4-(2,4-difluorophenyl)quinoline-6-carboxylate | HCID 67773515 | 69.3% |
Reaction Steps
Under argon gas atmosphere, a mixture of methyl 4-bromo-3-chloroquinoline-6-carboxylate (130 mg), 2,4-difluorophenylboric acid (137 mg), a 1,1′-bis(diphenylphosphino)ferrocene palladium (H) dichloride/dichloromethane complex (177 mg), cesium fluoride (197 mg), 1,4-dioxane (8 mL), and water (2 mL) was heated under stirring in an oil bath at 100° C. for one day. The reaction mixture was returned to room temperature, and water was added, and extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the resulting residue was purified under silica gel column chromatography (hexane/ethyl acetate) to obtain methyl 3-chloro-4-(2,4-difluorophenyl)quinoline-6-carboxylate (100 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853242B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-777a251daad84671af204320cfc450bb |
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| Source note | uspto-grants-2014_10 |
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