Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 237829Erstellt: 25. Oktober 2026

3-Methoxyphenol → 7-Methoxy-1,2,3,4,4a,9b-hexahydro-dibenzofuran

https://huagongshe.com/reaction/237829

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-MethoxyphenolHCID 9007—
Edukt1,3-CyclohexadieneHCID 11605—
KatalysatorSilver(I) trifluoromethanesulfonateHCID 76223—
LösungsmittelDichloromethaneHCID 6344—
Produkt7-Methoxy-1,2,3,4,4a,9b-hexahydro-dibenzofuranHCID 68525916—
Produkt7-Methoxy-1,2,3,4-tetrahydro-dibenzofuranHCID 68527647—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A solution of AuCl3 (0.303 g, 1.0 mmol) and AgOTf (0.770 g, 3.0 mmol) was stirred in anhydrous CH2Cl2 (150 mL) for 2 hours. 3-methoxy-phenol (2.48 g, 20 mmol) in CH2Cl2 (25 mL) was added, followed by addition of cyclohexadiene in CH2Cl2 (25 mL) at 40° C. over two hours. The reaction mixture was stirred at 40° C. overnight. The reaction mixture was passed through a silica gel plug. The filtrate was concentrated. The residue was purified by silica gel chromatography (5-30% CH2Cl2/heptane) to give 0.393 g of the title compound and 0.67 g of 7-methoxy-1,2,3,4-tetrahydro-dibenzofuran.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642603B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-879e9f50f5df4bb7858c6c8777c461c0
Quellennotizuspto-grants-2014_02