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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611402Generated: October 27, 2026

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

https://huagongshe.com/reaction/1611402

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% suspension in mineral oil; 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) and the reaction mixture is heated at 60° C. for 6 h. After a night at room temperature, the reaction mixture is poured into water (250 ml) and extracted with ethyl acetate, then dried (Na2SO4) The drying agent is filtered off and the solvent is evaporated off under reduced pressure. 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 numberUS06987122B2
Source datasetuspto-grants-2006_01
ORD IDord-e44e5c0371864af49c1dfd1a377acad9
Source noteuspto-grants-2006_01