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HRID 32251Erstellt: 25. Oktober 2026

1,2-Dimethoxyethane → 2-(3,3,5,5-Tetramethylcyclohex-1-enyl)phenol

https://huagongshe.com/reaction/32251

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DimethoxyethaneHCID 8071—
EduktSodium CarbonateHCID 10340—
Edukt2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 2734622—
Edukt3,3,5,5-Tetramethylcyclohex-1-en-1-yl triflateHCID 11087380—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt2-(3,3,5,5-Tetramethylcyclohex-1-enyl)phenolHCID 23142526101%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a mixture of 2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenol(3.5 g, 15.9 mmol), trifluoromethanesulfonic acid 3,3,5,5-tetramethylcyclohex-1-enyl ester (5 g, 17.4 mmol) produced in Example (4a) and 1,2-dimethoxyethane (20 mL) were added tetrakis(triphenylphosphine)palladium(0) (0.92 g, 0.79 mmol) and 2N aqueous solution of sodium carbonate (23.9 mL, 47.7 mmol), followed by stirring for 1 hour at an external temperature of 90° C. under a nitrogen atmosphere. Brine was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and then the solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (ethyl acetate/heptane) to give 3.7 g of the title compound as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425554B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-f1e3eb10a5b247ef95e4208d5352e5da
Quellennotizuspto-grants-2008_09