HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489987Generated: October 30, 2026
Ethanol → ethyl 1-ethyl-5-nitro-1H-indole-2-carboxylate
https://huagongshe.com/reaction/489987
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 5-nitro-1H-indole-2-carboxylate | HCID 280312 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 1-ethyl-5-nitro-1H-indole-2-carboxylate | HCID 12148796 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06979692B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-13501dd3bd5b4f519d0a30a10976668d |
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| Source note | uspto-grants-2005_12 |
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