反応 #2137804

ord-af4af4b61ec84ae4a532787f7581ba07

反応条件

温度
20°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出extracted three times with ethyl acetate
  2. 2
    乾燥the organic phases are dried over magnesium sulfate
  3. 3
    その他The solvent is evaporated off
  4. 4
    その他the crude product is purified by chromatography on silica gel

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05013847uspto-grants-1991_05