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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383483Erstellt: 24. Oktober 2026

(4-Methoxyphenyl)boronic acid → 4-(4-methoxyphenyl)-5,5-dimethylfuran-2(5H)-one

https://huagongshe.com/de/reaction/383483

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-Methoxyphenyl)boronic acidHCID 201262—
EduktPotassium FluorideHCID 522689—
Edukt2,2-Dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonateHCID 58926348—
KatalysatorBenzyl triethylammonium chlorideHCID 66133—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelToluene waterHCID 22272177—
Produkt4-(4-methoxyphenyl)-5,5-dimethylfuran-2(5H)-oneHCID 58926254—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a 1:1 mixture of toluene/water (20 mL), were added 2,2-dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate (100 mg, 0.38 mmol), 4-methoxyphenylboronic acid (87 mg, 0.57 mmol), PdCl2(PPh3)2 (27 mg, 0.038 mmol), 2M KF aqueous solution (0.95 mL, 1.9 mmol), benzyltriethylammonium chloride (8.7 mg, 0.038 mmol). The mixture was heated at 50° C. under N2 for 30 minutes, cooled to room temperature and extracted with EtOAc (2×50 mL). The organic layers were combined, washed with saturated NaHCO3 (50 mL) and brine (50 mL), dried over Na2SO4. Purification through silica gel column with 10-30% EtOAc/hexanes led to the product as yellow solid. Yield: 33 mg, 40%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367664B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-e2663724bba84f1bb0566abf2e0d5651
Quellennotizuspto-grants-2013_02