HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1747478Erstellt: 26. Oktober 2026
Iodoethane → 1-ethyl-4-methyl-1H-indole-3-carbaldehyde
https://huagongshe.com/reaction/1747478
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Iodoethane | HCID 6340 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-methyl-1H-indole-3-carbaldehyde | HCID 2762437 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-ethyl-4-methyl-1H-indole-3-carbaldehyde | HCID 59497237 | 63% |
Reaktionsschritte
To a solution of 4-methyl-1H-indole-3-carbaldehyde (150 mg. 0.942 mmol) in dry DMF (1 mL) was added NaH (26 mg, 1.08 mmol) in 3 portions. When the evolution of gas was complete, the reaction vial was sealed and agitated for 5 m, after which time ethyl iodide (0.086 mL, 1.1 mmol) was added and agitation was continued overnight. The mixture was diluted with dichloromethane (10 mL), washed with water (2×5 mL), and brine (5 mL), dried and concentrated. This mixture was purified by flash chromatography using a gradient of ethyl acetate/hexane to provide 1-ethyl-4-methyl-1H-indole-3-carbaldehyde (111 mg, 63%). This intermediate (371 mg, 2 mmol) was dissolved in THF (3 mL) and NaBH4 (38 mg, 5 mmol) was added followed by 3 drops of water. The reaction mixture was agitated for 4 h then added to a saturated solution of NaHCO3 (10 mL). This mixture was stirred for 1 h and the intermediate, (1-ethyl-4-methyl-1H-indol-3-yl)-methanol was isolated by filtration and dried (330 mg, 88% yield). This intermediate was then convened to the title compound using methods similar to those described in Example 31. LCMS (ESMS): m/z 420 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09150556B2 |
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| Quelldatensatz | uspto-grants-2015_10 |
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| ORD ID | ord-cce48957e34648ce9d86bb8a35591c58 |
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| Quellennotiz | uspto-grants-2015_10 |
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