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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Indole | HCID 798 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4,6-Trimethylbenzyl chloride | HCID 74108 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-[(2,4,6-Trimethylphenyl)methyl]-1H-indole | HCID 22256742 | 87.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06753342B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-879af4c043fb407ea9d2fc46a8361995 |
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| Source note | uspto-grants-2004_06 |
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