HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561021Generated: October 30, 2026
Potassium Phosphate, Tribasic → 5-Cyclopropyl-2-fluoropyridine
https://huagongshe.com/reaction/561021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 2-Fluoro-5-iodopyridine | HCID 2783179 | — |
| Reactant | Toluene water | HCID 22272177 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Chloroform isopropyl alcohol | HCID 21906603 | — |
| Product | 5-Cyclopropyl-2-fluoropyridine | HCID 57690831 | 63% |
Reaction Steps
In a flask, combine 2-fluoro-5-iodo-pyridine (1.12 g, 5 mmol), cyclopropylboronic acid (645 mg, 7.5 mmol), palladium acetate (56 mg, 0.25 mmol), potassium phosphate (3.2 g, 15 mmol), and toluene-water (20:1, 21 mL). Heat the mixture at 100° C. for 4 hours. Dilute the mixture with chloroform-isopropanol (3:1, 100 mL). Wash the organic phase with saturated aqueous sodium chloride and water. Dry the mixture over sodium sulfate. Concentrate the solution in vacuo to a brown oil. Purify by column chromatography (20% ethyl acetate in hexane) to afford the title compound (430 mg, 63%) as a pale yellow oil. 1H NMR (400 MHz-CDCl3) δ 7.99 (d, J=3 Hz, 1H), 7.39 (td, J=3, 5 Hz, 1H), 6.79 (dd, J=3, 8 Hz, 1H), 0.96-1.02 (m, 2H), 0.63-0.69 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063212B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-39fe37e08ab049d3a44aa8730b56f7b7 |
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| Source note | uspto-grants-2011_11 |
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