HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166055Generated: October 30, 2026
Ethyl 5-methoxyindole-2-carboxylate → Ethyl 5-hydroxy-1H-indole-2-carboxylate
https://huagongshe.com/reaction/1166055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 5-methoxyindole-2-carboxylate | HCID 20926 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 5-hydroxy-1H-indole-2-carboxylate | HCID 90677 | 48.2% |
Reaction Steps
Boron tribromide (64.58 g) was added dropwise to a stirred solution of ethyl 5-methoxyindole-2-carboxylate (20 g) in dry dichloromethane (1000 ml) at −78° C. under an atmosphere of argon. The reaction was allowed to warm to room temperature and stirred for a further 2 hours. The reaction was poured into ice/saturated aqueous sodium hydrogen carbonate solution with stirring and extracted with ethyl acetate. Combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution, water, aqueous saturated sodium chloride solution and dried (MgSO4). The solution was concentrated in vacuo and the residue was purified by column chromatography using 0-60% diethyl ether iso-hexane as eluent to give product as a white solid (9.02 g, 48%); NMR δ(CD3SOCD3) 1.31 (t, 3H), 4.29 (q, 2H), 6.79 (dd, 1H), 6.90 (dd, 1H), 7.22 (d, 1H), 8.84 (s, 1H), 11.52 (brs, 1H), M/z (+) 206 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613760B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-b927751d9faf46ed9523f7ab2659f177 |
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| Source note | uspto-grants-2003_09 |
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