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Acrylonitrile → (2-Cyanoethyl)-alpha-naphthoxymalonic acid diethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acrylonitrile | HCID 7855 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 4-Cyano-2(R,S)-alpha-naphthoxybutyric acid | HCID 23049648 | — |
| 反応物 | alpha-Naphthoxymalonic acid diethyl ester | HCID 54105534 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | (2-Cyanoethyl)-alpha-naphthoxymalonic acid diethyl ester | HCID 54279623 | — |
反応手順
4-Cyano-2(R,S)-α-naphthoxybutyric acid: 0.11 ml of a 50% aqueous KOH solution is added at 0°, while stirring, to a mixture of 5.0 g of α-naphthoxymalonic acid diethyl ester and 1.09 ml of acrylonitrile. The reaction mixture is stirred for 5 days at room temperature and then dissolved in ethyl acetate. The ethyl acetate solution is washed with 2N sodium bicarbonate solution, 2N hydrochloric acid and brine, dried over sodium sulphate and concentrated by evaporation, leaving (2-cyanoethyl)-α-naphthoxymalonic acid diethyl ester.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04727060 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-0c2d879632c7416297f9a04382172ffc |
| 出典メモ | uspto-grants-1988_02 |