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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042855Generated: October 30, 2026

Potassium Phosphate, Tribasic → 7-Chloro-2-cyclopropylfuro[3,2-b]pyridine

https://huagongshe.com/reaction/1042855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
ReactantHCID 66779473HCID 66779473—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product7-Chloro-2-cyclopropylfuro[3,2-b]pyridineHCID 59427325—

Reaction Conditions

Temperature100 °C

Reaction Steps

7-Chloro-2-iodofuro[3,2-b]pyridine (0.130 g, 0.47 mmol), cyclopropylboronic acid (0.080 g, 0.93 mmol), and tricyclohexylphosphine (0.026 g, 0.093 mmol) were dissolved in 3 mL toluene and 1 mL water. Potassium phosphate (0.30 g, 1.4 mmol) was added followed by PdOAc2 (0.010 g, 0.047 mmol), the reaction was flushed with argon, and the reaction stirred at 100° C. for 48 h. The reaction was cooled to RT and partitioned between DCM and water. The layers were separated and the aqueous layer was extracted with DCM. The combined organic layers were dried with sodium sulfate, filtered, and concentrated. The crude material was purified via column chromatography (gradient elution 0-50% EtOAc:Hex) to afford 7-chloro-2-cyclopropylfuro[3,2-b]pyridine as an orange oil. MS: M+H+=194.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557816B2
Source datasetuspto-grants-2013_10
ORD IDord-306d0a10b49f417b82208ed42912102c
Source noteuspto-grants-2013_10