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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225921Generated: October 30, 2026

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

https://huagongshe.com/reaction/225921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ProductN-Methyl-N-[(1-methyl-2-indolyl)methyl]acrylamideHCID 20752825—

Reaction Steps

To a solution of 1-methyl-2-methylaminomethyl)indole (0.96 g, 55 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 numberUS07557125B2
Source datasetuspto-grants-2009_07
ORD IDord-d26ed7f3f75c44699db0cb0c0e13016e
Source noteuspto-grants-2009_07