化工社化工社 化学情報印刷レポート · 研究参考用
Ethyl Acetate → 5-[(E)-2-phenylethenyl]-1,2,4-oxadiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | HCID 178520452 | HCID 178520452 | — |
| 溶媒 | HOAc dioxane | HCID 22565020 | — |
| 生成物 | 5-[(E)-2-phenylethenyl]-1,2,4-oxadiazole | HCID 22291342 | 8% |
反応手順
N-[(Hydroxyamino)methylene]-cinnamamide (850 mg, 4.5 mmol) was dissolved in acetic acid/dioxane (20 mL 1:1 v:v), and heated to reflux for 2 h. The cooled solution was made basic (pH 8) with K2CO3, and partitioned between ethyl acetate and water. The organics were dried over Na2SO4, and concentrated in vacuo. The resultant solids were triturated with hot ethyl acetate, and the soluble portion was purified by flash column chromatography on silica eluting with 2:1 hexane:ethyl acetate to afford 5-[(E)-2-phenylethenyl]-1,2,4-oxadiazole (60 mg, 8% yield) as a white powder. M.p. 53–55° C. 1H NMR (CDCl3, 300 MHz) δ8.43 (s, 1H), 7.85 (d, J=16 Hz, 1H), 7.60 (m, 2H), 7.45 (m, 3H), 7.05 (d, J=16 Hz, 1H). MS (EI ionization) 171 (M+−H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06956049B1 |
| 出典データセット | uspto-grants-2005_10 |
| ORD ID | ord-6ad1428dd2c64d83a156f20351cef2f1 |
| 出典メモ | uspto-grants-2005_10 |