HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929371Generated: November 1, 2026
Potassium Phosphate, Tribasic → 5-Cyclopropyl-2-fluoropyridine
https://huagongshe.com/reaction/1929371
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 5-Bromo-2-fluoropyridine | HCID 2783168 | — |
| Catalyst | HCID 178482626 | HCID 178482626 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Cyclopropyl-2-fluoropyridine | HCID 57690831 | — |
Reaction Steps
A mixture of 2-fluoro-5-bromopyridine (1.17 ml, 11.4 mmol), cyclopropylboronic acid (1.47 g, 17.1 mmol) and potassium phosphate (7.26 g, 34.2 mmol) in 1,4-dioxane (20 ml) was stirred under argon atmosphere. Chloro(di-2-norbornylphosphino)(2-dimethylaminoferrocen-1-yl)palladium(II) (67 mg, 0.11 mmol) was added. The reaction mixture was heated at 100° C. under argon atmosphere for 48 hours and then cooled down to room temperature. The crude mixture was partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography (ISCO Companion|, 80 g column, 0-10% EtOAc/Petroleum ether) to afford the compound (70:30 mixture product: starting material; 1.55 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188071B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-d2979cb93a8b43e59bb9e5bc946bb5aa |
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| Source note | uspto-grants-2012_05 |
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