HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18228Erstellt: 24. Oktober 2026
Methylamine → N-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amine
https://huagongshe.com/de/reaction/18228
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methylamine | HCID 6329 | — |
| Edukt | 3-Formyl-2-methylindole | HCID 73166 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amine | HCID 10954023 | 63% |
Reaktionsschritte
To a solution of 2-methylindole-3-carboxaldehyde (10.00 g, 62.84 mmole) in MeOH (100 mL) was added 2 M CH3NH2 in MeOH (200 mL). After stirring for 3 hours at RT, the reaction solution was concentrated to a yellow oil which solidified under vacuum. This solid was dissolved in ethanol (350 mL) and NaBH4 (2.38 g, 62.8 mmole) was added. The reaction was stirred at RT for 6 hours, then was concentrated under vacuum. The remaining residue was diluted with saturated aqueous Na2CO3 (50 mL) and extracted with EtOAc (2×200 mL). The organic phase was separated, washed with brine, and dried over Na2SO4. Flash chromatography on silica gel (9:1 CHCl3/MeOH containing 5% NH4OH) and drying under high vacuum gave the title compound (6.88 g, 63%) as a faintly yellow viscous solid: MS (ES) m/e 175 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741339B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-53d950d90541411399039216f0d61e5c |
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| Quellennotiz | uspto-grants-2010_06 |
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