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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249135Generated: October 29, 2026

Hydrochloric Acid → Ethyl 4-[3-(3-nitrobenzoyl)indol-1-yl]butyrate

https://huagongshe.com/reaction/249135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant3-m-NitrobenzoylindoleHCID 9838206—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 4-[3-(3-nitrobenzoyl)indol-1-yl]butyrateHCID 1054779390.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 3-(3-nitrobenzoyl)indole (2.09 g), ethyl 4-bromobutyrate (1.614 g) and potassium carbonate (3.118 g) in N,N-dimethylformamide (20 ml) was stirred at 25° C. overnight. The reaction mixture was poured into a mixture of ethyl acetate and 1N hydrochloric acid. The organic layer was separated, washed with water and brine, and dried over magnesium sulfate. After evaporation of solvent, the crystalline residue was recrystallized from a mixture of ethyl acetate and hexane to give ethyl 4-[3-(3-nitrobenzoyl)indol-1-yl]butyrate (2.71 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212320
Source datasetuspto-grants-1993_05
ORD IDord-725c85b05ef24bb495679ea3a2e1a18b
Source noteuspto-grants-1993_05