HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786453Generated: October 26, 2026
Boron tribromide → 6-Bromo-5-hydroxy-1H-indole-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1786453
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 6-Bromo-5-methoxyindole-2-carboxylate | HCID 14546582 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Bromo-5-hydroxy-1H-indole-2-carboxylic acid ethyl ester | HCID 67017907 | 72.2% |
Reaction Steps
A solution of 8.30 g (27.8 mmol) 6-bromo-5-methoxy-1H-indole-2-carboxylic acid ethyl ester (prepared according to J. Org. Chem. 1974, 39, 3580) in 160 mL dichloromethane was cooled to −78° C. At this temperature, 55.7 mL boron tribromide (55.7 mmol; 1M solution in dichloromethane) were added. The solution was allowed to warm to room temperature and after 30 min. the solution was poured into 10% aqueous sodium bicarbonate solution; the phases were separated and the aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed with water, brine, dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash chromatography on silica gel with n-hexane:ethyl acetate (2:1 v/v) as eluant to afford 5.7 g (72%) of the product as a light-yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507736B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-4dd177b61f4645da8471e1b54c07186b |
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| Source note | uspto-grants-2009_03 |
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