HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264627Generated: October 31, 2026
Sodium Chloride → 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carbaldehyde
https://huagongshe.com/reaction/2264627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | {1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}methanol | HCID 67044165 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carbaldehyde | HCID 44210807 | 98.4% |
Reaction Steps
To a solution of 0.93 g of {1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}methanol and 1.1 mL of triethylamine in 10 mL of 1,2-dichloroethane, a solution of 1.21 g of sulfur trioxide-pyridine complex in 5 mL of DMSO was added under ice cooling, and the resulting mixture was stirred under ice cooling for 1 hour. The solution was poured into a mixed solution of 25 ml of ice water and 25 mL of saturated aqueous sodium chloride solution, the resulting mixture was extracted with 100 mL of ethyl acetate, the extract was washed with 5% aqueous potassium hydrogen sulfate solution, water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was washed with hexane to obtain 0.91 g of 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carbaldehyde as a beige solid. FAB+: 364, 366
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-a18ca397aefb404880692ac250803299 |
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| Source note | uspto-grants-2010_12 |
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