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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 849362생성일: 2026년 10월 25일

4-Bromodiphenyl Ether → 1-(4-Phenoxyphenyl)propan-2-one

https://huagongshe.com/reaction/849362

반응식

참여 물질

역할이름HCID투입량
반응물4-Bromodiphenyl EtherHCID 7565—
반응물Isopropenyl acetateHCID 7916—
반응물Potassium FluorideHCID 522689—
반응물Methoxytri-n-butylstannaneHCID 11964040—
용매TolueneHCID 1140—
생성물1-(4-Phenoxyphenyl)propan-2-oneHCID 1959152383%

반응 단계

75.0 g of 4-bromodiphenyl ether, 129 ml of tributyltin methoxide, 45.0 g of isopropenyl acetate and 2,47 g of dichlorobis{tri(o-tolyl)phosphine}palladium, were dissolved in 300 ml of toluene and refluxed under heating for 3 hours. The reaction solution was left to cool to room temperature, and then, a saturated potassium fluoride aqueous solution was added, followed by stirring for one hour. Then, the product was subjected to celite filtration and washed with ethyl acetate. The filtrate and 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=15/1→10/1) to obtain 56.3 g (yield: 83%) 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-16f48f99f052458ab881bcbd42a77a81
출처 메모uspto-grants-2000_01