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Hydrochloric Acid → (2-Carbamoylethyl)-alpha-naphthoxymalonic acid diethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Acrylamide | HCID 6579 | — |
| 反応物 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 反応物 | 4-Carbamoyl-2(R,S)-alpha-naphthoxybutyric acid | HCID 23049649 | — |
| 反応物 | alpha-Naphthoxymalonic acid diethyl ester | HCID 54105534 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (2-Carbamoylethyl)-alpha-naphthoxymalonic acid diethyl ester | HCID 54384256 | — |
反応手順
4-Carbamoyl-2(R,S)-α-naphthoxybutyric acid: 1.49 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene are added to a solution of 3 g of α-naphthoxymalonic acid diethyl ester (Example 36a) and 0.71 g of acrylamide in 5 ml of acetonitrile and the whole is stirred at room temperature for 24 hours. 25 ml of water are added to the reaction mixture, which is adjusted to pH 2 with 2N hydrochloric acid and extracted with ether. The ethereal phases are washed with water and brine, dried over sodium sulphate and concentrated by evaporation, leaving (2-carbamoylethyl)-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-822d95ff4f2445239bc38f50ab6bd0a8 |
| 出典メモ | uspto-grants-1988_02 |