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HRID 2074434作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl Ethyl KetoneHCID 6569—
反応物Potassium CarbonateHCID 11430—
反応物4-Trifluoromethyl-8-propyl-7-hydroxycoumarinHCID 53701430—
反応物3-(4-Bromobutyl)-1,5,5-trimethylimidazolidine-2,4-dioneHCID 67089119—
溶媒WaterHCID 962—
生成物1,5,5-trimethyl-3-[4-[2-oxo-8-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy]butyl]imidazolidine-2,4-dioneHCID 57962786103.8%

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07919509B2
出典データセットuspto-grants-2011_04
ORD IDord-2a4c7284e12349bbb711d1dab2d8dd90
出典メモuspto-grants-2011_04