HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1033975Erstellt: 26. Oktober 2026
Hydrochloric Acid → (4-Bromophenyl)(4-fluorophenyl)methanone
https://huagongshe.com/reaction/1033975
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Fluorobenzene | HCID 10008 | — |
| Edukt | p-Bromobenzyl chloride | HCID 68528 | — |
| Edukt | 4-Fluoro-4'-(phenylethynyl)benzophenone | HCID 4095657 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Produkt | (4-Bromophenyl)(4-fluorophenyl)methanone | HCID 74951 | 86% |
Reaktionsschritte
Synthesis of 4-fluoro-4'-phenylethynylbenzophenone In a 250 mL flask equipped with a nitrogen inlet, overhead stirring assembly, and reflux condenser was placed fluorobenzene (117 g, 1.2 mol), and 4-bromobenzyl chloride (39.8 g, 0.181 mol). The mixture was cooled to 0° C. an anhydrous aluminum chloride (27 g, 0.20 mol) was added. The mixture was stirred at 23° C. for 16 hours. The resulting slurry was poured into 2 L of acidic (HCl) water. The organics were extracted with methylene chloride, and dried over magnesium sulfate. The slurry was filtered and the methylene chloride was removed under reduced pressure. Recrystallization from ethanol afforded 43.3 g (86%) of 4-bromo-4'-fluorobenzophenone as white crystals: mp 106°-107° C. (Lit 107°-108° C.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05312994 |
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| Quelldatensatz | uspto-grants-1994_05 |
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| ORD ID | ord-d03901bcb5e142568d70254e005582fc |
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| Quellennotiz | uspto-grants-1994_05 |
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