Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | methyl 1H-indole-4-carboxylate | HCID 2733668 | — |
| Edukt | Potassium sodium tartarate | HCID 9855836 | — |
| Edukt | Diisobutylaluminumhydride | HCID 21225700 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1H-indol-4-ylmethanol | HCID 2773457 | 101,5% |
Reaktionsschritte
Diisobutylaluminum hydride (1 M in toluene; 1.3 mL, 1.3 mmol) was added to a solution of 1H-indole-4-carboxylic acid, methyl ester (85 mg, 0.49 mmol) in ether (1.6 mL) at −70° C. The solution was allowed to stir at −70° C. for 1 h, then at room temperature for 1 h. Ethyl acetate (20 mL) was added, and the solution was stirred with an aqueous solution of potassium sodium tartrate (30% w/v; 20 mL) for 30 min. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried (MgSO4), filtered, evaporated, and dried under high vacuum to give 1H-indole-4-methanol (73.2 mg, quantitative yield) which was used in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06803384B2 |
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| Quelldatensatz | uspto-grants-2004_10 |
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| ORD ID | ord-43b8b6bb80274100a5fdb0ce735ba707 |
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| Quellennotiz | uspto-grants-2004_10 |
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