HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504789Generated: October 26, 2026
Citric Acid → 5-(2-methoxyethoxy)-7-nitro-1H-indole-2-carboxylic acid
https://huagongshe.com/reaction/504789
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | ethyl 5-(2-methoxyethoxy)-7-nitro-1H-indole-2-carboxylate | HCID 57476190 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 5-(2-methoxyethoxy)-7-nitro-1H-indole-2-carboxylic acid | HCID 57476219 | 97.2% |
Reaction Steps
Ethyl 5-(2-methoxyethoxy)-7-nitro-1H-indole-2-carboxylate (7.7 g) was dissolved in a mixed solvent of ethanol (75 mL) and tetrahydrofuran (75 mL), 1N aqueous sodium hydroxide solution (75 mL) was added to this solution, and the mixture was stirred at 50° C. for 1.5 hr. Aqueous citric acid solution was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, dried over magnesium sulfate, and filtrated, and the filtrate was concentrated under reduced pressure. The obtained crude product was crystallized from ethyl acetate-hexane to give the title compound (6.8 g, yield 97%) as yellow crystals. melting point 192-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07777047B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-3bce77e0a0ba4cfe8da4a80ce4a7dfe0 |
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| Source note | uspto-grants-2010_08 |
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