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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761116Generated: November 2, 2026

Triethylamine → N-Methyl-N-[(1-methyl-2-indolyl)methyl]acrylamide

https://huagongshe.com/reaction/1761116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactantmethyl((1-methyl-1H-indol-2-yl)methyl)amineHCID 11401058—
SolventDichloromethaneHCID 6344—
ProductN-Methyl-N-[(1-methyl-2-indolyl)methyl]acrylamideHCID 20752825—

Reaction Steps

To a solution of 1-methyl-2-(methylaminomethyl)indole (0.96 g, 5.5 mmole), from Preparation 1, and triethylamine (1.54 mL, 11.0 mmole) in CH2Cl2 (50 mL) at 5° C. was added acryloyl chloride (0.48 mL, 6.0 mmole). After 45 min, the reaction solution was poured onto H2O and the layers were separated. The organic phase was dried over Na2SO4 and concentrated to afford the title compound as a yellow oil. This was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846819B1
Source datasetuspto-grants-2005_01
ORD IDord-0528b58bfae24c0a90f62a6ac3ddf137
Source noteuspto-grants-2005_01