HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976722Generated: October 26, 2026
Hydrochloric Acid → 6-Methoxy-1H-indole-3-carboxaldehyde
https://huagongshe.com/reaction/1976722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-Methoxy-1H-indole | HCID 76659 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Methoxy-1H-indole-3-carboxaldehyde | HCID 907214 | 69% |
Reaction Steps
A mixture of DMF (7 mL, 90 mm) and POCl3 (2.25 mL, 24.5 mmol) which had been cooled to 5° C., was treated with known 6-methoxy-1H-indole. After stirring at room temperature for 1 hour, the mixture was heated at 45° C. for 1 hour, then allowed to cool to room temperature overnight. The reaction mixture was poured into ice (100 mL), and stirred for 30 minutes at which time a solution of KOH (9.6 g, 171 mm) in H2O (20 mL) was added dropwise. After stirring for 30 minutes, then heating for 1 hour at 60° C., the reaction was cooled to 30° C., and the pH adjusted to 7 with 1N HCl. The mixture was extracted with EtOAc(50 mL×3), the organic fractions were combined, dried over MgSO4, filtered and evaporated. The residue was purified by crystallization from methanol to afford 6-methoxy-1H-indole-3-carboxaldehyde (1.65 g, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06228877B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-5c4db0a1b92543749ca98c104f1e7f5d |
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| Source note | uspto-grants-2001_05 |
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