HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1532458Erstellt: 27. Oktober 2026
1-Iodonaphthalene → 1-[2-(Benzenesulfonyl)ethenyl]naphthalene
https://huagongshe.com/reaction/1532458
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Iodonaphthalene | HCID 7004 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-(Phenylsulfonyl)ethanol | HCID 30202 | — |
| Edukt | Tri-o-tolylphosphine | HCID 80271 | — |
| Edukt | Methanesulfonic anhydride | HCID 81560 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-[2-(Benzenesulfonyl)ethenyl]naphthalene | HCID 70222497 | 66% |
Reaktionsschritte
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, 0.22 ml (1.5 mmol) of 1-iodonaphthalene, 0.11 g (0.05 mmol) of palladium acetate, and 0.067 g (0.22 mmol) of tri(o-tolyl)phosphine were added thereto, 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=80/20) to obtain 0.194 g of [2-(phenylsulfonyl)ethenyl]naphthalene. Yield: 66%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06201131B1 |
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| Quelldatensatz | uspto-grants-2001_03 |
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| ORD ID | ord-1b2a7b12718245e689cb4fa35de28d90 |
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| Quellennotiz | uspto-grants-2001_03 |
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