HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 616270Erstellt: 25. Oktober 2026
Acetic Anhydride → Alpha-acetamido-6-methylindole-3-acrylic acid ethylester
https://huagongshe.com/reaction/616270
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | 2-Acetamido-3-ethoxy-3-oxopropanoic acid | HCID 3276255 | — |
| Edukt | 6-Methylindole-3-carboxaldehyde | HCID 4777902 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | Alpha-acetamido-6-methylindole-3-acrylic acid ethylester | HCID 54175825 | 89% |
Reaktionsschritte
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 1 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°).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04073795 |
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| Quelldatensatz | uspto-grants-1978_02 |
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| ORD ID | ord-e133900a9c3641189a1bfb2f1c91b88c |
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| Quellennotiz | uspto-grants-1978_02 |
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