Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182475Generated: October 25, 2026

2,3-Dihydrofuran → 2-(3,4,5-Trimethoxyphenyl)-2,3-dihydrofuran

https://huagongshe.com/reaction/2182475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DihydrofuranHCID 70934—
Reactant5-Iodo-1,2,3-trimethoxybenzeneHCID 298133—
ReactantPotassium AcetateHCID 517044—
CatalystTriphenylphosphineHCID 11776—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(3,4,5-Trimethoxyphenyl)-2,3-dihydrofuranHCID 2247895243.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 5-iodo-1,2,3-trimethoxybenzene (900 mg, 3.06 mmol) and 2,3-dihydrofuran (1.16 mL, 15.3 mmol) in dry DMF (8 mL) were added PPh3 (20 mg, 0.077 mmol), KOAc (901 mg, 9.18 mmol), n-Bu4NCl (850 mg, 3.06 mmol) and Pd(OAc)2 (17 mg, 0.077 mmol). The reaction mixture was stirred 18 h at 80° C. The reaction mixture was diluted with AcOEt and water. After separation, the organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. The crude residue was then purified by flash chromatography on silica gel (AcOEt/Hexane: 20/80) to afford the title compound 287 (311 mg, 1.32 mmol, 43% yield). 1H NMR: (300 MHz, CDCl3) δ (ppm): 6.59 (s, 2H), 6.45 (m, 1H), 5.45 (dd, J=10.5, 8.4 Hz, 1H), 4.97 (m, 1H), 3.87 (s, 6H), 3.84 (s, 3H), 3.06 (m, 1H), 2.62 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897220B2
Source datasetuspto-grants-2005_05
ORD IDord-25289407e3f4449e98c724f372e44de0
Source noteuspto-grants-2005_05