関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | 2-Acetamido-3-ethoxy-3-oxopropanoic acid | HCID 3276255 | — |
| 反応物 | 6-Methylindole-3-carboxaldehyde | HCID 4777902 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | Alpha-acetamido-6-methylindole-3-acrylic acid ethylester | HCID 54175825 | 89% |
反応手順
A 3-l. three-necked flask, equipped with a mechanical stirrer, a thermometer and a dropping funnel with pressure-equalizing arm was charged with 100 g (0.63 mol) of 6-methylindole-3-carboxaldehyde, 119 g (0.63 mol) of acetamidomalonic acid monoethylester and 500 ml of pyridine. The mixture was stirred and kept at 15° with a cold water bath while 175 ml of acetic anhydride was added over 15 minutes. The yellow solution was stirred at room temperature for 3 hours. Then an additional portion of 36 g (0.19 mol) of acetamidomalonic acid monoethyl ester was added and stirring at room temperature was continued for 22 hours before 1 kg of ice was added. The temperature fell to -10° and the product began to precipitate. The suspension was stirred at room temperature for 5 hours and poured into 2 l of water. After 20 minutes, the precipitate was collected by suction filtration, washed with water and dried at 50° in an air oven overnight to afford 159.5 g (89%) of crude product as yellow crystals, m.p. 159°-162° (sinters at 75°).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04256641 |
|---|
| 出典データセット | uspto-grants-1981_03 |
|---|
| ORD ID | ord-2ab58062813f4f47b10284910e356cfd |
|---|
| 出典メモ | uspto-grants-1981_03 |
|---|