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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093385Generated: October 26, 2026

Acetonitrile → 1-(2-fluoro-5-methylphenyl)-3-(tetrahydro-2H-pyran-2-yloxy)-1-propyne

https://huagongshe.com/reaction/1093385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantCesium carbonateHCID 10796—
Reactant3-Bromo-4-fluorotolueneHCID 96745—
ReactantTetrahydro-2-(2-propynyloxy)-2H-pyranHCID 98609—
CatalystBis(acetonitrile)dichloropalladiumHCID 6093782—
Catalyst2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
SolventSodium chloride; waterHCID 57417360—
Product1-(2-fluoro-5-methylphenyl)-3-(tetrahydro-2H-pyran-2-yloxy)-1-propyneHCID 59407681—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3-bromo-4-fluorotoluene (10.0 g), cesium carbonate (45.0 g), 2-(2-propynyloxy)tetrahydropyran (11.2 ml), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (1.51 g), bis(acetonitrile)palladium(II) dichloride (274 mg) and acetonitrile (250 ml) was stirred at 90° C. for 11 hr. The reaction mixture was added to brine, and the mixture was extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=99:1-95:5) to give the object product (8.32 g) as a pale-brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129361B2
Source datasetuspto-grants-2012_03
ORD IDord-91fa2044eb65491d9106fee2a1efd413
Source noteuspto-grants-2012_03