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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353470Generated: October 25, 2026

Indole → 1-[(2,4,6-Trimethylphenyl)methyl]-1H-indole

https://huagongshe.com/reaction/353470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2,4,6-Trimethylbenzyl chlorideHCID 74108—
SolventDimethyl SulfoxideHCID 679—
Product1-[(2,4,6-Trimethylphenyl)methyl]-1H-indoleHCID 2225674287.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of indole (1.185 g) in dry DMSO (3 ml) is dropped into a suspension of sodium hydride (60% mineral oil suspension; 0.44 g) in dry DMSO (10 ml). After two hours, the resulting solution is added with a solution of 2,4,6-trimethylbenzyl chloride (1.9 g) in dry DMSO (2 ml) heating at 60° C. for 6 h. The reaction mixture is kept at room temperature overnight, then poured into water (250 ml) extracted with ethyl acetate and dried (Na2SO4). The drying agent is filtered off, the solvent is evaporated off under reduced pressure and the resulting residue is purified by column chromatography (silica gel; eluent n-hexane/AcOEt 9/1) to obtain 2.2 g of 1-(2,4,6-trimethylbenzyl)indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753342B2
Source datasetuspto-grants-2004_06
ORD IDord-879af4c043fb407ea9d2fc46a8361995
Source noteuspto-grants-2004_06