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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1033975Erstellt: 26. Oktober 2026

Hydrochloric Acid → (4-Bromophenyl)(4-fluorophenyl)methanone

https://huagongshe.com/reaction/1033975

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktFluorobenzeneHCID 10008—
Eduktp-Bromobenzyl chlorideHCID 68528—
Edukt4-Fluoro-4'-(phenylethynyl)benzophenoneHCID 4095657—
EduktAluminum(III) ChlorideHCID 6451240—
Produkt(4-Bromophenyl)(4-fluorophenyl)methanoneHCID 7495186%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05312994
Quelldatensatzuspto-grants-1994_05
ORD IDord-d03901bcb5e142568d70254e005582fc
Quellennotizuspto-grants-1994_05