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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18245Erstellt: 24. Oktober 2026

Triethylamine → N-(1H-indol-3-ylmethyl)-N-methylacrylamide

https://huagongshe.com/de/reaction/18245

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAcryloyl chlorideHCID 13140—
EduktN-Methyl-1H-indole-3-methanamineHCID 96388—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(1H-indol-3-ylmethyl)-N-methylacrylamideHCID 2213914780,7%

Reaktionsschritte

Acryloyl chloride (0.33 mL, 4.10 mmole) was added to a solution of 3-(methylaminomethyl)-1H-indole (0.60 g, 3.70 mmole) and Et3N (1.03 mL, 7.40 mmole) in CH2Cl2 (30 mL) at 0° C. The reaction was held at 0° C. for ten minutes, then was stirred overnight at RT. The solution was concentrated in vacuo and the residue was diluted with water. The solution was extracted with ethyl acetate, and the combined organic extracts were washed with brine and dried over Na2SO4. The title compound (0.64 g, 80%) was obtained as a light yellow solid: MS (ES) m/e 215 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741339B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-33cd541701934d24bbc4faf3aa66cc7b
Quellennotizuspto-grants-2010_06