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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710569Generated: November 2, 2026

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

https://huagongshe.com/reaction/1710569

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 (0.78 g, 4.5 mmole), from Preparation 1, and triethylamine (1.4 mL, 10.0 mmole) in CH2Cl2 (50 mL) at 5° C. was added acryloyl chloride (0.41 mL, 4.95 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 numberUS07790716B2
Source datasetuspto-grants-2010_09
ORD IDord-6b67032b1bae4b2e8bf8ed75581df73c
Source noteuspto-grants-2010_09