HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480067Generated: October 31, 2026
Tetrahydrofuran → 5-Chloro-3-methyl-1H-indole-2-carboxylic acid
https://huagongshe.com/reaction/480067
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1H-Indole-2-carboxylic acid, 5-chloro-3-methyl-, ethyl ester | HCID 949859 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Chloro-3-methyl-1H-indole-2-carboxylic acid | HCID 3159706 | — |
Reaction Steps
2N NaOH (20 mL) was added to a suspension of 5-chloro-3-methyl-1H-indole-2-carboxylic acid ethyl ester (7.0 g, 29.4 mmol) in methanol (50 mL) and the resulting mixture stirred at 25° C. for 18 hours. Tetrahydrofuran (100 mL) was added and the resulting solution heated at reflux for 30 minutes and concentrated. The residue was dissolved in water and the resulting solution extracted twice with ethyl acetate. The aqueous layer was acidified and the precipitate collected by filtration and washed with water (5.24 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06649634B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-f015c50c841643678696f71adf269ac7 |
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| Source note | uspto-grants-2003_11 |
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