化工社化工社 化学情報印刷レポート · 研究参考用
3,5-Diiodosalicylic acid → N-[3-chloro-5-methyl-4-[1-(4-chlorophenyl)ethenyl]phenyl]-3,5-diiodo-2-hydroxybenzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,5-Diiodosalicylic acid | HCID 8631 | — |
| 反応物 | Phosphorus trichloride | HCID 24387 | — |
| 反応物 | 1-(4-Amino-2-chloro-6-methylphenyl)-1-(4-chlorophenyl)ethylene | HCID 23323150 | — |
| 生成物 | N-[3-chloro-5-methyl-4-[1-(4-chlorophenyl)ethenyl]phenyl]-3,5-diiodo-2-hydroxybenzamide | HCID 23323149 | — |
反応手順
Using the reaction sequence of Example 4, 3,5-diiodosalicylic acid is reacted with 1-(4-amino-2-chloro-6-methylphenyl)-1-(4-chlorophenyl)ethylene in the presence of phosphorus trichloride to give N-[3-chloro-5-methyl-4-[1-(4-chlorophenyl)ethenyl]phenyl]-3,5-diiodo-2-hydroxybenzamide. The benzophenone used as starting material for the Wittig reaction was prepared by reacting 4-chlorobenzyl cyanide with 3-chloro-5-methyl-1-nitrobenzene followed by oxidation with alkaline peroxide as known in the literature.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04587361 |
| 出典データセット | uspto-grants-1986_05 |
| ORD ID | ord-91459bcd657c4ad9b89aeb1ee04995d5 |
| 出典メモ | uspto-grants-1986_05 |