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HRID 377761作成日:2026年10月26日
4-(Methylsulfonyl)benzaldehyde → (Z)-5-methoxy-2-methyl-1-(p-methylsulfonylbenzylidene)-3-indenylacetic acid
https://huagongshe.com/reaction/377761
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-(Methylsulfonyl)benzaldehyde | HCID 220376 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | Methyl 5-methoxy-2-methyl-3-indenylacetate | HCID 53634864 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (Z)-5-methoxy-2-methyl-1-(p-methylsulfonylbenzylidene)-3-indenylacetic acid | HCID 70286603 | — |
反応手順
25% methanolic sodium methoxide (16 ml, 2.0 equivalents) is treated with a solution of methyl 5-methoxy-2-methyl-3-indenylacetate (from Example 4, Part C) (8.7 g; 0.037 mol) and p-methylsulfonylbenzaldehyde, (6.3 g; 1.1 equivalent). The mixture is stirred at reflux under nitrogen for 2 hours. An equal volume of water is added slowly, and refluxing is continued for 30 min. The solution is cooled, is diluted with water and is washed with ether. Residual ether is blown off with nitrogen. The aqueous solution is acidified with 10% hydrochloric acid. The precipitated product is collected and is washed thoroughly with water. The crude product is crystallized from methanol to give (Z)-5-methoxy-2-methyl-1-(p-methylsulfonylbenzylidene)-3-indenylacetic acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06028116 |
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| 出典データセット | uspto-grants-2000_02 |
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| ORD ID | ord-113586e271734fa8a1342d6dff985c0c |
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| 出典メモ | uspto-grants-2000_02 |
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