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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368912Generated: October 30, 2026

Iodobenzene → 2-phenyl-2,3-dihydrofuran

https://huagongshe.com/reaction/368912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodobenzeneHCID 11575—
ReactantTriphenylphosphineHCID 11776—
Reactant2,3-DihydrofuranHCID 70934—
ReactantPotassium AcetateHCID 517044—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-phenyl-2,3-dihydrofuranHCID 1088805258%

Reaction Steps

Table 1, Entry 5. In the reaction tube were mixed iodobenzene (0.102 g, 0.5 mmol), dihydrofuran (0.350 g, 5.0 mmol), palladium acetate (0.00281 g, 0.0125 mmol), potassium acetate (0.147 g,1.5 mmol), n-Bu4NCl (0.139 g, 0.5 mmol), triphenylphosphine (0.00328 g, 0.0125 mmol) and 1.0 ml DMF.under nitrogen. The contents of the flask were irradiated for 6.00 min with an effect of 60 W. After cooling, the product mixture was poured into 25 ml water and was extracted three times with 25 ml DCM. The combined extracts were washed with 25 ml water and concentrated to an oil. The crude product was purified by column chromatography on silica gel using pentaneldiethyl ether (19/1) as the eluent. The yield was 58% (yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136157
Source datasetuspto-grants-2000_10
ORD IDord-ecee3b0fcc474c9593d591808a029019
Source noteuspto-grants-2000_10