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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant2-Fluoro-5-iodopyridineHCID 2783179—
ReactantToluene waterHCID 22272177—
Catalystpalladium(II) acetateHCID 167845—
SolventChloroform isopropyl alcoholHCID 21906603—
Product5-Cyclopropyl-2-fluoropyridineHCID 5769083163%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063212B2
Source datasetuspto-grants-2011_11
ORD IDord-39fe37e08ab049d3a44aa8730b56f7b7
Source noteuspto-grants-2011_11