HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303386Generated: October 31, 2026
Indole → 1-[(4-Nitrophenyl)methyl]-1H-indole
https://huagongshe.com/reaction/2303386
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | 4-Nitrobenzyl chloride | HCID 7482 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-[(4-Nitrophenyl)methyl]-1H-indole | HCID 4289225 | — |
Reaction Steps
A mixture of 5.28 g of sodium hydride (0.22 mol, mineral oil suspension) in 200 ml of dimethyl sulfoxide is treated with a solution of 23.4 g (0.2 mol) of indole in 100 ml of dimethyl sulfoxide. It is heated at 65° C. for 1 hour, then allowed to cool and 37.7 g (0.22 mol) of 4-nitrobenzyl chloride are then added dropwise. The solution is heated to 60° C., kept at room temperature for 14 hours and then poured into 700 ml of ater with stirring. The mixture is extracted in portions with a total of 300 ml of methylene chloride, the organic phase is dried using anhydrous sodium sulfate, filtered and the filtrate is concentrated in vacuo. The residue is purified on a silica gel column (silica gel 60, Merck AG, Darmstadt; eluent methylene chloride/ethanol 9:1, v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432987B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-ac9dc70d65a549738a824bc0ae7f2c70 |
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| Source note | uspto-grants-2002_08 |
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