HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1673253Erstellt: 24. Oktober 2026
Ethanone, 1-(2-chlorophenyl)- → 2-[4-Chloro-3-(methyloxy)phenyl]-1-(2-chlorophenyl)-ethanone
https://huagongshe.com/de/reaction/1673253
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanone, 1-(2-chlorophenyl)- | HCID 72864 | — |
| Edukt | 2-(Dicyclohexylphosphino)-2'-methylbiphenyl | HCID 2734938 | — |
| Edukt | 5-Bromo-2-chloroanisole | HCID 2769567 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-[4-Chloro-3-(methyloxy)phenyl]-1-(2-chlorophenyl)-ethanone | HCID 67330467 | — |
Reaktionsschritte
A mixture of 1-(2-chlorophenyl)ethanone (1.4 mL, 10.8 mmol), 4-bromo-1-chloro-2-(methyloxy)benzene (2.0 g, 9.0 mmol), sodium tert-butoxide (2.2 g, 22.6 mmol), palladium(II) acetate (20.3 mg, 0.1 mmol), and 2-(dicyclohexylphosphino)-2′-methylbiphenyl (65.8 mg, 0.2 mmol) in 30 mL of toluene was degassed and stirred at 80° C. for 16 h. The reaction mixture was cooled and a mixture of Et2O (100 mL) and H2O (100 mL) was added. The aq layer was separated and extracted with Et2O (3×50 mL). Organic layers were combined, dried over MgSO4, and concentrated. Chromatography on a Biotage 40+M cartridge using 1:9 v/v EtOAc/hexanes as the eluant afforded the product: 1H NMR δ 3.87 (s, 3H), 4.22 (s, 2H), 6.75 (dd, J=1.7, 8.2, 1H), 6.81 (d, J=1.6, 1H), 7.26-7.31 (m, 2H), 7.37-7.43 (m, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07999107B2 |
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| Quelldatensatz | uspto-grants-2011_08 |
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| ORD ID | ord-232b8803963f40f0a7456c432aca91f1 |
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| Quellennotiz | uspto-grants-2011_08 |
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