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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactant4-Nitrobenzyl chlorideHCID 7482—
ReactantSodium hydrideHCID 24758—
SolventDimethyl SulfoxideHCID 679—
Product1-[(4-Nitrophenyl)methyl]-1H-indoleHCID 4289225—

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432987B1
Source datasetuspto-grants-2002_08
ORD IDord-ac9dc70d65a549738a824bc0ae7f2c70
Source noteuspto-grants-2002_08