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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602237Erstellt: 24. Oktober 2026

Anisole → 4'-Methoxyacetophenone

https://huagongshe.com/de/reaction/602237

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnisoleHCID 7519—
EduktAcetic AnhydrideHCID 7918—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
Edukt3-Trifluoromethyl-5-trifluoromethanesulfonyl-1,2,4-triazoleHCID 178527382—
KatalysatorScandiumHCID 23952—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelNitromethaneHCID 6375—
Produkt4'-MethoxyacetophenoneHCID 747697,2%

Reaktionsbedingungen

Temperatur21 °C

Reaktionsschritte

The catalytic effect of the scandium salt of 3-trifluoromethyl-5-trifluoromethanesulfonyl-1,2,4-triazole, obtained in Example 3, relative to a reaction was evaluated in the following manner. In 40 ml of anhydrous nitromethane, there is added 592 mg (700 .mu.moles) of the scandium salt of 3-trifluoromethyl-5-trifluoromethanesulfonyl-1,2,-4-triazole, and 1.08 g (10 mmoles) of anisol and 2.04 g of acetic anhydride. After stirring during 10 min at 21° C., the reaction mixture was diluted with 50 ml of ether and the reaction was inhibited by 100 ml of a saturated solution of sodium bicarbonate NaHCO3. After filtration on Celite, the solution was extracted with three fractions of 50 ml ether, and the collected ether phase was washed with a saturated solution of potassium chloride. After drying the ether phase with magnesium sulfate and evaporation, 1.46 g of p -methoxyacetophenone (97% yield) was collected, with a purity characterized by a proton NMR higher than 99%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07906235B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-0f4f1a9a186a4902a9a8aeae64d7416f
Quellennotizuspto-grants-2011_03