HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339042Generated: October 25, 2026
Water → 8-(Difluoromethoxy)-6-fluoro-2-methylquinoline
https://huagongshe.com/reaction/339042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-2,2-difluoroacetophenone | HCID 238296 | — |
| Reactant | 6-Fluoro-8-hydroxy-2-methylquinoline | HCID 66781517 | — |
| Product | 8-(Difluoromethoxy)-6-fluoro-2-methylquinoline | HCID 70984374 | — |
Reaction Steps
To a mixture of 6-fluoro-2-methylquinolin-8-ol (0.15 g, 0.85 mmol) and potassium carbonate (4.2 g, 30 mmol) in acetonitrile (3.4 mL, 0.85 mmol) and water (3.4 mL, 0.85 mmol) was added 2-chloro-2,2-difluoroacetophenone (0.62 mL, 4.2 mmol). The vessel was sealed and the mixture was heated at 80° C. for 4 hours. The cooled reaction mixture was extracted with diethyl ether (2×30 mL), and the combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure at ambient temperature The resulting residue was purified by reverse phase chromatography on a C18 column (0-100% acetonitrile/water). Aqueous fractions containing the product were combined and extracted with diethyl ether (2×100 mL). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure at ambient temperature providing the title compound. Presence of water was noted and the material taken on as is assuming theoretical yield obtained (0.19 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889704B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-75c94b7ae1fc4b6fba7882526e3a2fab |
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| Source note | uspto-grants-2014_11 |
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