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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455821Generated: October 31, 2026

Ethanol → ethyl 1-ethyl-5-nitro-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1455821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 5-nitro-1H-indole-2-carboxylateHCID 280312—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productethyl 1-ethyl-5-nitro-1H-indole-2-carboxylateHCID 12148796—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Nitro-1H-indole-2-carboxylic acid ethyl ester (5 g, 21.3 mol) was dissolved in DMF (50 mL). The reaction mixture was cooled to 0° C. Sodium hydride (1.02, 25.5 mmol, 60% in mineral oil) was added to the above solution in portions over 10 minutes. The mixture was stirred at room temperature for 30 minutes. Ethyl iodide (6.5 g, 42 mmol) was added to the above solution and the reaction mixture was stirred overnight. Ethanol (30 mL) was added to the reaction mixture and the mixture was poured into cold water (800 mL). The crude product was collected by filtration and used directly in next step without further purification (5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482368B2
Source datasetuspto-grants-2009_01
ORD IDord-26849391ca4440e49824e2dbf186be1a
Source noteuspto-grants-2009_01