HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25332Generated: October 25, 2026
Hydrochloric Acid → 4-Hydroxyindole-3-carboxaldehyde
https://huagongshe.com/reaction/25332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1H-indol-4-ol | HCID 75421 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Hydroxyindole-3-carboxaldehyde | HCID 9815282 | 82% |
Reaction Steps
Phosphorous oxychloride 7.35 ml was added dropwise to dry dimethylformamide 15 ml under cooling in ice-methanol bath and the mixture was stirred for 15 min. Then, a solution of the 4-hydroxyindole 5.0 g in dry dimethylformamide 10 ml was added dropwise to the mixture under cooling in ice and the mixture was stirred for 2 h at room temperature. Water was added under cooling in ice to the mixture, which was made alkaline with a 30% aqueous sodium hydroxide solution and was stirred for 15 min. Then, the mixture was acidified to pH 4 with 5N-HCl and the precipitate was collected by filtration, washed with water and dried to give the titled compound 4.99 g as crude crystalline materials. Yield 82%. Crude crystalline materials are recrystallized from methanol to give yellow crystals m.p. 190-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858640B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-2970d5c5affd4345a64be8337930ba6f |
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| Source note | uspto-grants-2005_02 |
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