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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1163270Erstellt: 26. Oktober 2026

Phenol, 4-bromo-, 1-acetate → Triacetylresveratrol

https://huagongshe.com/reaction/1163270

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenol, 4-bromo-, 1-acetateHCID 74726—
EduktSodium BicarbonateHCID 516892—
Edukt3,5-Diacetoxy StyreneHCID 11310559—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
ProduktTriacetylresveratrolHCID 5962587—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A flask equipped with magnetic stirrer was charged with 50 mg (0.23 mmol, 1 eq) of 3,5-diacetoxystyrene, 49 mg (0.23 mmol) of 4-acetoxybromobenzene, 46 mg (0.27 mmol) of NaHCO3 and 78 mg (0.54 mmol, 2.4 eq) of tetrabutylammoniumchloride. The reactants were suspended in 2 ml DMF and the mixture was flushed with argon and then evacuated. The argon flushing and evacuation procedure was carried out three times. The reaction was started by adding 0.76 mg of palladium acetate in 50 μl of de-aerated DMF (3 μmol, 1.5 mol %), and stirred at 100° C. for three hours. Work-up of the reaction mixture following the procedure of Example 5 gave (E)-3,4′,5-triacetoxystilbene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07820848B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-c1bbab8e0da74da3ae16839899640c2c
Quellennotizuspto-grants-2010_10