HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169355Generated: November 4, 2026
Potassium Carbonate → ethyl 6-(4-methylphenyl)-1H-indole-2-carboxylate
https://huagongshe.com/reaction/1169355
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Bromo-1H-indole-2-carboxylic acid ethyl ester | HCID 7009496 | — |
| Reactant | 4-Methylphenyl dihydrogen borate | HCID 19035350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol toluene water | HCID 86587398 | — |
| Product | ethyl 6-(4-methylphenyl)-1H-indole-2-carboxylate | HCID 22990151 | 75.1% |
Reaction Steps
A mixture of ethyl 6-bromo-1H-indole-2-carboxylate (2.5 g) and 4-methylphenylboric acid (1.39 g), potassium carbonate (2.58 g) and toluene/ethanol/water (90/9/9 ml) was stirred at room temperature for one hour. Into the reaction mixture was added tetrakis(triphenylphosphine)palladium (0.32 g), and the resulting mixture was heated at reflux for 18 hours. After cooling to room temperature, the mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated solution of sodium chloride and was dried with magnesium sulfate. After concentration under reduced pressure, the residue was subjected to purification using column chromatography (ethyl acetate/hexane 1:5→1:2→1:1) and to recrystallization (ethyl acetate/hexane) to obtain ethyl 6-(4-methylphenyl)-1H-indole-2-carboxylate (1.92 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06627651B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-09fb8bc2a9b44f5e965601581d9830ee |
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| Source note | uspto-grants-2003_09 |
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