HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 873474Erstellt: 24. Oktober 2026
Methanol → 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylic acid
https://huagongshe.com/de/reaction/873474
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methanol | HCID 887 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | methyl 6-cyano-1-isopropyl-3-methyl-1H-indole-4-carboxylate | HCID 67467281 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylic acid | HCID 67468089 | 64,2% |
Reaktionsschritte
To a 50 ml round bottom was added methyl 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylate (230 mg, 0.897 mmol), followed by methanol (1 mL) and THF (1 mL). To the solution was added 3 M NaOH (0.449 mL, 2.69 mmol). The reaction stirred at rt for 20 h. The reaction was evaporated and treated with acidic water to pH 5. A brown solid crashed out and was collected by filtration. The solid was an impurity. The pH of the liquid was adjusted to 3 and the liquid was evaporated leaving a residue. Trituration of the residue with water, followed by filtration yielded 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylic acid (155 mg, 0.576 mmol, 64.2% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-δ6) δ ppm 13.16 (br. s., 1 H) 8.33 (s, 1 H) 7.78 (s, 1 H) 7.66 (s, 1 H) 4.81-4.98 (m, 1 H) 2.33 (s, 4 H) 1.45 (d, J=6.57 Hz, 6 H). MS(ES) [M+H]+ 243.3.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08975291B2 |
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| Quelldatensatz | uspto-grants-2015_03 |
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| ORD ID | ord-8b224ac6470d4db7b5f9e395aaf662ff |
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| Quellennotiz | uspto-grants-2015_03 |
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