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HRID 2074434Erstellt: 26. Oktober 2026

Methyl Ethyl Ketone → 1,5,5-trimethyl-3-[4-[2-oxo-8-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy]butyl]imidazolidine-2,4-dione

https://huagongshe.com/reaction/2074434

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl Ethyl KetoneHCID 6569—
EduktPotassium CarbonateHCID 11430—
Edukt4-Trifluoromethyl-8-propyl-7-hydroxycoumarinHCID 53701430—
Edukt3-(4-Bromobutyl)-1,5,5-trimethylimidazolidine-2,4-dioneHCID 67089119—
LösungsmittelWaterHCID 962—
Produkt1,5,5-trimethyl-3-[4-[2-oxo-8-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy]butyl]imidazolidine-2,4-dioneHCID 57962786103,8%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A 2-butanone (2 mL) solution of 7-hydroxy-8-propyl-4-(trifluoromethyl)-2H-chromen-2-one (30 mg, 0.11 mmol), 3-(4-bromobutyl)-1,5,5-trimethylimidazolidine-2,4-dione (30.5 mg, 0.11 mmol), and potassium carbonate (22.8 mg, 0.165 mmol) was heated and stirred overnight at 80° C. The reaction solution was added with water and extracted with ethyl acetate. Subsequently, the organic layer was washed with saturated saline, dried using anhydrous sodium sulfate, and concentrated under vacuum. The obtained residue was purified using thin-layer silica-gel chromatography (hexane:ethyl acetate=1:1), and 53.5 mg of the title compound (yield 100%) was obtained as colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07919509B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-2a4c7284e12349bbb711d1dab2d8dd90
Quellennotizuspto-grants-2011_04