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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18235Erstellt: 24. Oktober 2026

Methylamine → N-Methyl-1H-indole-3-methanamine

https://huagongshe.com/de/reaction/18235

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
EduktIndole-3-CarboxaldehydeHCID 10256—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
ProduktN-Methyl-1H-indole-3-methanamineHCID 96388—

Reaktionsschritte

To a solution of indole-3-carboxaldehyde (5.4 g, 34.1 mmole) in MeOH (30 mL) was added a solution of 2.0 M CH3NH2 in MeOH (51.3 mL, 102.6 mmole). The reaction was stirred at RT overnight, then was concentrated to a light yellow oil. This oil was dissolved in EtOH (40 mL), and NaBH4 (1.3 g, 34.1 mmole) was added. After 16 hrs the reaction was concentrated to a slurry and dissolved in 10% Na2CO3(100 mL). The aqueous solution was extracted with EtOAc (2×200 mL) and the combined organic fractions were dried over Na2SO4 and concentrated. Drying in high vacuum left the title compound (5.2 g, 94%) as a faintly yellow oil: MS (ES) m/e 161 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741339B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-45b3fc57b00a46048def2730ac9a2839
Quellennotizuspto-grants-2010_06