HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626043Generated: November 1, 2026
Dichloromethane → 2-Fluoro-6-(5-fluoro-2-methoxy-4-vinylphenoxy)pyridine
https://huagongshe.com/reaction/626043
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 5233012 | — |
| Reactant | 2-(4-Bromo-5-fluoro-2-methoxyphenoxy)-6-fluoropyridine | HCID 59191227 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Fluoro-6-(5-fluoro-2-methoxy-4-vinylphenoxy)pyridine | HCID 59191319 | — |
Reaction Steps
To 2-(4-bromo-5-fluoro-2-methoxyphenoxy)-6-fluoropyridine (227 mg, 0.71 mmol) were added [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (58.9 mg, 0.07 mmol) and potassium carbonate (597 mg, 4.26 mmol). To the mixture were added acetonitrile (4 mL), water (1.3 mL) and vinyl boronic acid pinacol ester (180 μL, 1.07 mmol). The reaction was flushed with argon, and left to stir for 3 days at 60° C. The reaction mixture was then filtered on celite, rinsed with dichloromethane and concentrated. After purification by preparative TLC (cyclohexane/ethyl acetate: 70/30), the title product was isolated as an orange oil (166 mg, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309179B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-19e3a439a6da4b60b9b3e5578199598d |
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| Source note | uspto-grants-2016_04 |
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