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HRID 52863作成日:2026年10月23日

Isopropenyl acetate → 2-Fluoro-4-biphenylyl acetone

https://huagongshe.com/ja/reaction/52863

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropenyl acetateHCID 7916—
反応物4-Bromo-2-fluoro-1,1'-biphenylHCID 521063—
反応物Potassium FluorideHCID 522689—
反応物Tributyltin butoxideHCID 18005932—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物2-Fluoro-4-biphenylyl acetoneHCID 1295041878%

反応条件

温度80 °C

反応手順

150 g of 4-bromo-2-fluorobiphenyl, 89.6 g of isopropenyl acetate, 258 ml of tributyltin butoxide and 4.7 g of a palladium chloride-tri(o-phenyl)phosphine complex were added to 300 ml of toluene and the mixture was stirred under heating at 80° C. for 2 hours under a nitrogen atmosphere. The reaction solution was left to cool to room temperature. Then, 1 l of ethyl acetate and 500 ml of a saturated potassium fluoride aqueous solution were added thereto, and the mixture was vigorously stirred. Insoluble matters were separated by filtration, and then the organic layer was collected by separation. The obtained organic layer was post-treated by a conventional method. The product was treated with hexane to obtain 106 g (yield: 78%) of 1-(2-fluoro-4-biphenylyl)-2-propanone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616803
出典データセットuspto-grants-1997_04
ORD IDord-78364f8d075a4580b40cb96512755919
出典メモuspto-grants-1997_04