HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372688Generated: November 2, 2026
Hydrochloric Acid → 1-ethyl-1H-indole-3-carboxylic acid
https://huagongshe.com/reaction/1372688
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 1-ethylindole-3-carboxylate | HCID 5191495 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-ethyl-1H-indole-3-carboxylic acid | HCID 3697160 | 90% |
Reaction Steps
In THF (9.0 ml) was dissolved the methyl 1-ethylindole-3-carboxylate obtained in the above-described (Step 1). To the resulting solution was added 0.25N NaOH (9.0 ml) at room temperature. After the reaction mixture was stirred at 50° C. for 36 hours, 1N NaOH (1.0 ml) was added thereto, followed by stirring at 70° C. for 9 hours. The reaction mixture was cooled to room temperature, and then neutralized with 1N HCl (4.5 ml). The crystals thus precipitated were collected by filtration under reduced pressure, washed with water and dried under reduced pressure to give 1-ethylindole-3-carboxylic acid (388.0 mg, 90%, yield of 2 steps) as a pale pink amorphous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-af1ffb82734b4e67a4e8e17d95ece895 |
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| Source note | uspto-grants-2007_01 |
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