関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Iodine | HCID 807 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Hydrogen iodide | HCID 24841 | — |
| 反応物 | 5-(3-Ethoxypropyl)-5-hydroxy-dibenzo[a,d]cycloheptene | HCID 23328862 | — |
| 生成物 | 5-(3-iodopropyl)-5H-dibenzo[a,d]cycloheptene | HCID 23328868 | — |
反応手順
A solution of 9.25 g. (0.0314 mole) of 5-(3-ethoxypropyl)-5-hydroxy-dibenzo[a,d]cycloheptene prepared as above in 45 ml. of acetic anhydride is heated on the steam-bath for 90 minutes then cooled to 65°C. A stream of nitrogen is passed through the solution while 30 ml. of hydriodic acid (sp. gr., 1.5) is added in portions, keeping the temperature below 90°C. The solution develops a dark brown iodine color during the addition. The solution is heated to 80°C. for 30 minutes, then cooled and poured into ice-water. The brown oil that separates is extracted into benzene and the extract washed with water, dilute sodium thiosulfate solution and finally with water. Evaporation of the benzene gives the product 5-(3-iodopropyl)-5H-dibenzo[a,d]cycloheptene as a yellow oil. A sample gives a precipitate with alcoholic silver nitrate solution.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US03981917 |
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| 出典データセット | uspto-grants-1976_09 |
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| ORD ID | ord-a239d11b41624253ba5c857b8b30a755 |
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| 出典メモ | uspto-grants-1976_09 |
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