HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197538Generated: November 1, 2026
Ethyl Acetate → 5-Bromo-2-fluoro-3-phenylpyridine
https://huagongshe.com/reaction/2197538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | 5-Bromo-2-fluoropyridine-3-boronic Acid (contains varying amounts of Anhydride) | HCID 2783242 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Bromo-2-fluoro-3-phenylpyridine | HCID 12033012 | 49.8% |
Reaction Steps
A solution of 5-bromo-2-fluoropyridin-3-ylboronic acid (620 mg, 2.82 mmol) and 1-iodobenzene (292 μL, 2.6 mmol) in 1,4-dioxane (50 μL) was degassed via nitrogen bubble for 15 mins. Then the mixture was added Pd(PPh3)4 (150 mg, 0.13 mmol) and aqueous Na2CO3 (24 μL, 5.7 mmol) and heated to 90° C. for 30 mins. The reaction was cooled to room temperature and poured into ethyl acetate (50 mL). The mixture was extracted with ethyl acetate, dried over Na2SO4, filtered and concentrated. The residue was purified via a flash column using 10% ethyl acetate in hexanes as an eluent. The product containing fractions were concentrated to give 5-bromo-2-fluoro-3-phenylpyridine (2.2) (326 mg, 49.8% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338604B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-fa54fb5d8d144999af6023db67bd3fe0 |
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| Source note | uspto-grants-2012_12 |
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