Zurück
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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethylamineHCID 6329—
EduktSodium borohydrideHCID 4311764—
Edukt1-methyl-1H-indole-5-carbaldehydeHCID 7537534—
LösungsmittelMethanolHCID 887—
Produktn-Methyl-1-(1-methyl-1h-indol-5-yl)methanamineHCID 1852575345%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07879872B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-00c2ad85f56b4055a48316a99d331c20
Quellennotizuspto-grants-2011_02