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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1710551Erstellt: 27. Oktober 2026

Sodium borohydride → [(1,2-dimethyl-1H-indol-3-yl)methyl](methyl)amine

https://huagongshe.com/reaction/1710551

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt1,2-Dimethyl-3-(methyliminomethyl)-1H-indoleHCID 14142219—
LösungsmittelEthanolHCID 702—
Produkt[(1,2-dimethyl-1H-indol-3-yl)methyl](methyl)amineHCID 1087790768%

Reaktionsschritte

1,2-Dimethyl-3-(methyliminomethyl)-1H-indole was taken up in ethanol (200 mL) and NaBH4 (2.6 g, 68.7 mmole) was added portionwise with stirring at RT (vigorous gas evolution). After 16 h the reaction was concentrated under vacuum, and the residue was basified with aqueous 1.0 N NaOH (200 mL). The mixture was extracted with Et2O (250 mL), and the combined Et2O extracts were washed with brine, dried (Na2SO4) and concentrated. Purification by flash chromatography on silica gel (5-10% (5% NH4OH/MeOH)/CHCl3) gave the title compound (8.47 g, 68%) as an oil which solidified in the freezer: 1H NMR (400 MHz, CDCl3) δ 7.60 (d, J=7.7 Hz, 1H), 7.29 (d, J=8.0 Hz, 1H), 7.19 (t, 1H), 7.12 (t, 1H), 3.93 (s, 2H), 3.69 (s, 3H), 2.49 (s, 3H), 2.45 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07790716B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-5cabe43a12ce45d7b2fc778fb5c3f716
Quellennotizuspto-grants-2010_09