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HRID 1033975作成日:2026年10月27日

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

https://huagongshe.com/reaction/1033975

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物FluorobenzeneHCID 10008—
反応物p-Bromobenzyl chlorideHCID 68528—
反応物4-Fluoro-4'-(phenylethynyl)benzophenoneHCID 4095657—
反応物Aluminum(III) ChlorideHCID 6451240—
生成物(4-Bromophenyl)(4-fluorophenyl)methanoneHCID 7495186%

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05312994
出典データセットuspto-grants-1994_05
ORD IDord-d03901bcb5e142568d70254e005582fc
出典メモuspto-grants-1994_05