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HRID 1742833作成日:2026年10月25日

Water → 5-[4-(Sec-butyloxy)-phenoxymethyl]-3-cyclopropyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/1742833

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物4-(1-Methyl-1-propyloxy)-phenolHCID 13882004—
反応物5-(Chloromethyl)-3-cyclopropyl-1,2,4-oxadiazoleHCID 15924311—
溶媒DimethylformamideHCID 6228—
生成物5-[4-(Sec-butyloxy)-phenoxymethyl]-3-cyclopropyl-1,2,4-oxadiazoleHCID 1465010877.2%

反応条件

温度20 °C

反応手順

5 g of 4-(sec-butyloxy)-phenol and 6.2 g of potassium carbonate are stirred in 50 ml of anhydrous dimethylformamide for 1 hour at 80° C. Subsequently, 4.8 g of 5-chloromethyl-3-cyclopropyl-1,2,4-oxadiazole in 20 ml anhydrous dimethylformamide is dripped in and the mixture stirred for 8 hours at 80° C. and overnight at room temperature (about 20° C.). The mixture is then poured into 100 ml of water and extracted three times with ethyl acetate, and the organic phases are dried over magnesium sulfate. The solvent is evaporated off and the crude product is purified by chromatography on silica gel using n-hexane/ethyl acetate (4:1) as eluant. There is obtained 6.7 g of 5-[4-(sec-butyloxy)-phenoxymethyl]-3-cyclopropyl-1,2,4-oxadiazole as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05342849
出典データセットuspto-grants-1994_08
ORD IDord-2e722019f3ff4dd3a065c63982dc8b53
出典メモuspto-grants-1994_08