HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478197Generated: October 30, 2026
Water → 3-Bromo-1-(P-toluenesulfonyl)indole
https://huagongshe.com/reaction/478197
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Bromo-1h-indole | HCID 2763277 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-Bromo-1-(P-toluenesulfonyl)indole | HCID 11210274 | 96% |
Reaction Steps
To a solution of 3-bromoindole (prepared according to the method described in Synthesis, 1096(1982)) (196 mg, 1.0 mmol) and tosyl chloride (286 mg, 1.5 mmol) in benzene (4.5 mL) was added tetra-n-butylammonium hydrogensulfate (34 mg, 0.1 mmol) and a 5.0% aqueous sodium hydroxide (1.0 mL), and the resulting mixture was refluxed for 1 hour. After the reaction solution was cooled to room temperature, water was added to the reaction solution, and the resulting mixture was extracted with chloroform. After drying over anhydrous sodium sulfate, the chloroform layer was concentrated, and the resulting crude product was purified by column chromatography on a silica gel (eluent; hexane:ethyl acetate=6:1) to afford the title compound (335 mg, yield: 96%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06642228B1 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-d4eccb9a4fc145d0b357794e9d169fb4 |
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| Source note | uspto-grants-2003_11 |
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