HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1362371Erstellt: 25. Oktober 2026
Water → n-Methyl-1-(1-methyl-1h-indol-5-yl)methanamine
https://huagongshe.com/reaction/1362371
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Methylamine | HCID 6329 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 1-methyl-1H-indole-5-carbaldehyde | HCID 7537534 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | n-Methyl-1-(1-methyl-1h-indol-5-yl)methanamine | HCID 18525753 | 45% |
Reaktionsschritte
1-Methyl-1H-indole-5-carbaldehyde (338 mg, 2.13 mmol) was dissolved in anhydrous methanol (10 ml). Methylamine (0.80 ml of 33% solution in ethanol, 6.43 mmol) was added and the reaction was stirred for 3 h. The solution was concentrated to a brown oil and then dissolved in anhydrous methanol (10 ml). Sodium borohydride (83.0 mg, 2.19 mmol) was added and the mixture was stirred overnight at room temperature. Water (4 ml) was added and the solution was concentrated. Sodium hydroxide (8 ml, 1N) was added and the aqueous layer was extracted with ethyl acetate (3×20 ml). Combined organic layers were dried over MgSO4, filtered and concentrated to afford methyl-(1-methyl-1H-indol-5-ylmethyl)-amine (167 mg, 45%) as an orange oil: 1H NMR (400 MHz, DMSO-d6) δ 7.44 (s, 1H), 7.34 (d, J=8.0 Hz, 1H), 7.261 (d, J=3.2 Hz, 1H), 7.11 (d, J=12.0 Hz, 1H), 6.345 (d, J=4.0 Hz, 1H), 3.75 (s, 3H), 3.70 (s, 2H), 2.25 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07879872B2 |
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| Quelldatensatz | uspto-grants-2011_02 |
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| ORD ID | ord-00c2ad85f56b4055a48316a99d331c20 |
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| Quellennotiz | uspto-grants-2011_02 |
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