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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15690Erstellt: 25. Oktober 2026

Vinyl propanoate → 4-Hydroxy-2-vinyloxyphenyl phenyl ketone

https://huagongshe.com/reaction/15690

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVinyl propanoateHCID 7750—
Edukt2,4-DihydroxybenzophenoneHCID 8572—
EduktSodium CarbonateHCID 10340—
Edukt[4-(Ethenyloxy)-2-hydroxyphenyl](phenyl)methanoneHCID 22935772—
LösungsmittelTolueneHCID 1140—
Produkt4-Hydroxy-2-vinyloxyphenyl phenyl ketoneHCID 22935793—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a mixture of di-μ-chlorobis(1,5-cyclooctadiene)diiridium(I) [Ir(cod)Cl]2 (1.27 g, 1.9 mmol) and sodium carbonate (24.9 g, 0.23 mol)) in toluene (280 ml) were added 2,4-dihydroxybenzophenone (40 g, 0.19 mol) and vinyl propionate (75.1 g, 0.75 mol), followed by stirring at 100° C. in an atmosphere of argon gas for 3 hours. The reaction mixture was analyzed by gas chromatography to find that 2-hydroxy-4-vinyloxyphenyl phenyl ketone [i.e., 2-hydroxy-4-vinyloxyphenyl(phenyl)methanone] and 4-hydroxy-2-vinyloxyphenyl phenyl ketone [i.e., 4-hydroxy-2-vinyloxyphenyl(phenyl) methanone] were formed in yields of 90% and 2%, respectively, with a conversion from 2,4-dihydroxybenzophenone of 99%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732645B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-444ed4c93c324f169126fe5d39585d30
Quellennotizuspto-grants-2010_06