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HRID 252771Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/252771

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-DihydrofuranHCID 70934—
Edukt5-Iodo-1,2,3-trimethoxybenzeneHCID 298133—
EduktPotassium AcetateHCID 517044—
KatalysatorTriphenylphosphineHCID 11776—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(3,4,5-Trimethoxyphenyl)-2,3-dihydrofuranHCID 2247895243,1%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07868204B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-a67bdf6bf52946058e0828fd58bfd8d7
Quellennotizuspto-grants-2011_01