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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880093Generated: October 26, 2026

Water → 4-(2-Fluoropyridin-3-YL)tetrahydro-2H-pyran-4-carbaldehyde

https://huagongshe.com/reaction/1880093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant3-Bromo-2-fluoropyridineHCID 2762778—
ReactantTetrahydro-2H-pyran-4-carboxaldehydeHCID 9964078—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product4-(2-Fluoropyridin-3-YL)tetrahydro-2H-pyran-4-carbaldehydeHCID 59327031—

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a sealed tube was added tetrahydro-2H-pyran-4-carbaldehyde (0.25 g, 2.190 mmol), 3-bromo-2-fluoropyridine (0.321 g, 1.825 mmol), palladium(ii) acetate (0.016 g, 0.073 mmol), cesium carbonate (0.714 g, 2.190 mmol), water (1.644 μL, 0.091 mmol), BINAP (0.068 g, 0.110 mmol) in Dioxane (7.30 mL). The resulting mixture was heated to 100° C. overnight. More catalyst and ligand (palladium(ii) acetate (0.016 g, 0.073 mmol), binap (0.068 g, 0.110 mmol)) were added and the resulting mixture was heated to 113° C. until the starting material was completely consumed. Aqueous work up followed by DCM extraction. Purification by Biotage (0-100% MeOH/DCM) & prep-plate TLC (5% MeOH/DCM) produced product which was advanced to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318718B2
Source datasetuspto-grants-2012_11
ORD IDord-e439a6c834c74dce87f31df40b9e8303
Source noteuspto-grants-2012_11