HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532456Generated: October 26, 2026
Triethylamine → 5-[2-(Phenylsulfonyl)ethenyl]indole
https://huagongshe.com/reaction/1532456
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Bromoindole | HCID 24905 | — |
| Reactant | 2-(Phenylsulfonyl)ethanol | HCID 30202 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Methanesulfonic anhydride | HCID 81560 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-[2-(Phenylsulfonyl)ethenyl]indole | HCID 54328560 | 23.3% |
Reaction Steps
To 0.186 g (1.0 mmol) of 2-(phenylsulfonyl)ethanol, 3 ml of acetonitrile was added, followed by 0.19 g(1.1 mmol) of methanesulfonic anhydride and 0.56 ml (4.0 mmol) of triethylamine, and the mixture was stirred for 5 hours at an internal temperature of 50° C. Subsequently, 0.29 g (1.5 mmol) of 5-bromoindole, 0.011 g (0.05 mmol) of palladium acetate, and 0.067 g (0.22 mmol) of tri(o-tolyl)phosphine were added, and the mixture was then refluxed for 17 hours. After cooled to room temperature, the reaction mixture was concentrated and purified by column chromatography (hexane/ethyl acetate=70/30) to obtain 0.066 g of 5-[2-(phenylsulfonyl)ethenyl]indole. Yield: 23%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06201131B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-90fb7022e82a4cb485d643bf37510e97 |
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| Source note | uspto-grants-2001_03 |
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