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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172219Generated: November 1, 2026

Water → HCID 70873440, compound

https://huagongshe.com/reaction/2172219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2H-Pyran, tetrahydro-2-(4-iodophenoxy)-HCID 2916803—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 69553293HCID 69553293—
Catalystpalladium(II) acetateHCID 167845—
CatalystTri-t-butylphosphine fluoroborateHCID 44558591—
SolventTolueneHCID 1140—
ProductHCID 70873440HCID 7087344086%

Reaction Steps

2-(4-Iodophenoxy)tetrahydropyran (1.12 g, 3.7 mmol) and 4-[3-(4-trifluoromethylphenyl)propyl]piperidine (1 g, 3.7 mmol) were dissolved in degassed anhydrous toluene (10 ml). Sodium tert-butoxide (0.50 g, 5.2 mmol), tri-tert-butylphosphine tetrafluoroborate (tBu3P.HBF4) (0.09 g, 0.3 mmol) and palladium acetate (0.03 g, 0.15 mmol) were added thereto, and the mixture was heated at reflux under a nitrogen atmosphere for 5 hours. After being allowed to cool to room temperature, water (10 ml) was added to the mixture, followed by extraction with ethyl acetate. The organic layers were combined and washed with water and a saturated sodium chloride aqueous solution, and dried over anhydrous sodium sulfate. After removing insoluble matter by filtration, the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=80:20) to afford the title compound as a pale yellow solid (1.42 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051333B2
Source datasetuspto-grants-2015_06
ORD IDord-139ad16ffecc460386d756a67bcb1d8d
Source noteuspto-grants-2015_06