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HRID 849376생성일: 2026년 10월 25일

Isopropenyl acetate → 2-Fluoro-4-biphenylyl acetone

https://huagongshe.com/reaction/849376

반응식

참여 물질

역할이름HCID투입량
반응물Isopropenyl acetateHCID 7916—
반응물4-Bromo-2-fluoro-1,1'-biphenylHCID 521063—
반응물Potassium FluorideHCID 522689—
반응물Methoxytri-n-butylstannaneHCID 11964040—
용매TolueneHCID 1140—
생성물2-Fluoro-4-biphenylyl acetoneHCID 12950418—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06011174
출처 데이터셋uspto-grants-2000_01
ORD IDord-5ff20dfa283b45cd9c16cda02f7dc8d9
출처 메모uspto-grants-2000_01