関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 3-Fluoro-4-(5-pentyl-1,3-dioxan-2-yl)-benzoic acid | HCID 20162499 | — |
| 生成物 | 3-Fluoro-4-(5-pentyl-1,3-dioxan-2-yl)-benzonitrile | HCID 20162157 | — |
反応手順
As described in Example 9 4.44 gms. of 3-fluoro-4-(5-pentyl-1,3-dioxan-2-yl)-benzoic acid are converted by SOCl2 into the acid chloride. After removing excess SOCl2 the residue obtained is added to aqueous ammonia and stirred for 4 hours at 20° C. The precipitated acid amide is filtrated by suction and dried. For conversion into the nitrile it is dissolved in 50 ml of pyridine and 10 ml of POCl3, then stirred at 20° C. for 20 hours and evaporated. Thus 3-fluoro-4-(5-pentyl-1,3-dioxan-2-yl)-benzonitrile is obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04704227 |
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| 出典データセット | uspto-grants-1987_11 |
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| ORD ID | ord-b642ce8d36d54bfcaaa5052a39948671 |
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| 出典メモ | uspto-grants-1987_11 |
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