関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-(1-Methyl-1-propyloxy)-phenol | HCID 13882004 | — |
| 反応物 | 5-(Chloromethyl)-3-cyclopropyl-1,2,4-oxadiazole | HCID 15924311 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-[4-(Sec-butyloxy)-phenoxymethyl]-3-cyclopropyl-1,2,4-oxadiazole | HCID 14650108 | 77.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05342849 |
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| 出典データセット | uspto-grants-1994_08 |
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| ORD ID | ord-2e722019f3ff4dd3a065c63982dc8b53 |
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| 出典メモ | uspto-grants-1994_08 |
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