HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264625Generated: October 31, 2026
p-Bromobenzenesulfonyl chloride → ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate
https://huagongshe.com/reaction/2264625
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Ethyl indole-2-carboxylate | HCID 73125 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate | HCID 67043967 | 95.3% |
Reaction Steps
To a solution of 0.5 g of potassium t-butoxide and 0.1 g of 18-crown-6 in 3 mL of THF, a mixed solution of 0.7 g of ethyl 1H-indole-2-carboxylate and 3 mL of THF was added, and the resulting mixture was stirred at room temperature for 30 minutes. The solution was cooled with ice, 1.13 g of 4-bromobenzenesulfonyl chloride was added, and the resulting mixture was stirred at room temperature for 5 hours. To the solution was added 60 mL of ethyl acetate, the resulting mixture was washed with water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-hexane=1:5) to obtain 1.44 g of ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate as a pale yellow syrup. FAB+: 408, 410
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855225B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-d6d5cf222d6e411eb1e67403140e4b05 |
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| Source note | uspto-grants-2010_12 |
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