HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1161884Erstellt: 24. Oktober 2026
Acetic Acid → 4-Amino-5-chloro-2-methyl-indole-1-carboxylic acid methyl ester
https://huagongshe.com/de/reaction/1161884
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 5-Chloro-2-methyl-4-nitro-indole-1-carboxylic acid methyl ester | HCID 66820264 | — |
| Katalysator | Iron | HCID 23925 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-Amino-5-chloro-2-methyl-indole-1-carboxylic acid methyl ester | HCID 66819957 | — |
Reaktionsschritte
5-Chloro-2-methyl-4-nitro-indole-1-carboxylic acid methyl ester (2.1 g, 7.81 mmol) is dissolved in ethanol (40 ml) and glacial acetic acid (40 ml). Iron powder (1.74 g, 31.26 mmol, activated previously with H2SO4 conc and then washed with water) is added, and the reaction mixture is heated to 85° C. for 90 minutes. The reaction mixture is poured into water and stirred at RT for 30 minutes, after which a slightly brownish colored precipitate forms which is filtered off. After washing with water and drying, the title compound is obtained in pure form. 1H NMR (DMSO, 400 MHz, 120° C.) δ 2.51 (s, 3H), 4.05 (s, 3H), 5.0-5.2 (br s, 2H), 6.66 (s, 1H), 7.05 (d, J=9 Hz, 1H), 7.31 (d, J=9 Hz, 1H); ES-MS: 238 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07820672B2 |
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| Quelldatensatz | uspto-grants-2010_10 |
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| ORD ID | ord-d5a07c42aa6c43d09299c5f96a3180f3 |
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| Quellennotiz | uspto-grants-2010_10 |
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