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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | 3-m-Nitrobenzoylindole | HCID 9838206 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 4-[3-(3-nitrobenzoyl)indol-1-yl]butyrate | HCID 10547793 | 90.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212320 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-725c85b05ef24bb495679ea3a2e1a18b |
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| Source note | uspto-grants-1993_05 |
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