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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249134Generated: October 29, 2026

Indole → 3-m-Nitrobenzoylindole

https://huagongshe.com/reaction/249134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantBenzoyl chloride, 3-nitro-HCID 8495—
ReactantEthyl AcetateHCID 8857—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product3-m-NitrobenzoylindoleHCID 983820634.8%

Reaction Steps

A solution of 3-nitrobenzoyl chloride (4.76 g) in dichloromethane (20 ml) was added to a suspension of aluminum chloride (3.42 g) in dichloromethane (50 ml) at 25° C., and the mixture was stirred at the same temperature for an hour. A solution of indole (3.0 g) in dichloromethane (20 ml) was added to the mixture at 25° C. After stirring for an hour at 25° C., the reaction mixture was poured into a mixture of ethyl acetate and ice water. The organic layer was separated, washed with water, and dried over magnesium sulfate. After evaporation of solvent, the crystalline residue was recrystallized from ethyl acetate to give 3-(3-nitrobenzoyl)indole (2.37 g) as pale red crystals. The mother liquid was purified by column chromatography on silica gel (20 g) with chloroform as eluent to give another crystals of 3-(3-nitrobenzoyl)indole (0.277 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212320
Source datasetuspto-grants-1993_05
ORD IDord-948135161ad247c08442bfa41733fbe7
Source noteuspto-grants-1993_05