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HRID 849376作成日:2026年10月26日

Isopropenyl acetate → 2-Fluoro-4-biphenylyl acetone

https://huagongshe.com/reaction/849376

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Methoxytri-n-butylstannaneHCID 11964040—
溶媒TolueneHCID 1140—
生成物2-Fluoro-4-biphenylyl acetoneHCID 12950418—

反応手順

15.0 g of 4-bromo-2-fluorobiphenyl, 25.8 ml of tributyltin methoxide, 8.96 g of isopropenyl acetate and 0.47 g of dichlorobis{tri(o-tolyl)phosphine}palladium, were dissolved in 100 ml of toluene and refluxed under heating for 2 hours. The reaction solution was left to cool to room temperature, and a saturated potassium fluoride aqueous solution was added, followed by stirring for one hour. Then the solution was subjected to celite filtration and washed with ethyl acetate. The filtrate and the washing liquid were put together. Then, the organic layer was separated and washed with a saturated sodium chloride aqueous solution and then, dried over anhydrous magnesium sulfate. The drying agent was filtered off, and then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1→5/1), followed by treatment with methylene chloride-hexane, to obtain 10.6 g of the above identified compound as yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06011174
出典データセットuspto-grants-2000_01
ORD IDord-5ff20dfa283b45cd9c16cda02f7dc8d9
出典メモuspto-grants-2000_01