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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1855361Erstellt: 27. Oktober 2026

Methanol → 4,4,4-Trifluoro-1-(4-pyrazol-1-yl-phenyl)-butane-1,3-dione

https://huagongshe.com/reaction/1855361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktEthyl trifluoroacetateHCID 9794—
EduktSodium MethoxideHCID 10942334—
Edukt1-[4-(1H-pyrazol-1-yl)phenyl]ethan-1-oneHCID 12238134—
LösungsmittelEthyl tert-butyl etherHCID 12512—
Produkt4,4,4-Trifluoro-1-(4-pyrazol-1-yl-phenyl)-butane-1,3-dioneHCID 6863093763,4%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A 5.4 N solution of sodium methoxide in methanol (3.0 mL, 16.2 mmol) was added drop wise over 10 min to a solution of ethyl trifluoro-acetate (1.81 mL, 15.2 mmol) in 2-ethoxy-2-methyl-propane (20 mL) at 20° C. followed by the addition of a suspension of 1-(4-pyrazol-1-yl-phenyl)-ethanone (2.57 g, 13.8 mmol) in 2-ethoxy-2-methyl-propane (10 mL). The reaction mixture was stirred for 22 h at 20° C. and then poured onto ice-water (50 mL). The mixture was extracted with ethyl acetate and the organic layer was washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The remaining solid was recrystallized from ethyl acetate/heptane to give the title compound (2.47 g, 63%) as off-white solid. Mp 96° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08962834B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-35d4d44f7e334382a8d9b1f824d5df5c
Quellennotizuspto-grants-2015_02