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
Participants
| Role | Name | HCID | Charge |
|---|
| 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% 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06987122B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-e44e5c0371864af49c1dfd1a377acad9 |
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| Source note | uspto-grants-2006_01 |
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