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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7472생성일: 2026년 10월 23일

Acetovanillone → 1-(4-Benzyloxy-3-methoxy-phenyl)-ethanone

https://huagongshe.com/ko/reaction/7472

반응식

참여 물질

역할이름HCID투입량
반응물AcetovanilloneHCID 2214—
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(4-Benzyloxy-3-methoxy-phenyl)-ethanoneHCID 9921599%

반응 단계

The starting material, 4-benzyloxy-3-methoxyacetophenone, was obtained by heating a solution of 4-hydroxy-3-methoxyacetophenone (20 g, 0.12 mol), benzyl bromide (15.7 ml, 0.13 mol) and potassium carbonate (49.8 g, 0.36 mol), in DMF (400 ml) at 40° C. overnight. After cooling, the mixture was diluted with water, acidified to approximately pH3 and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and the solvent evaporated. The residue was purified by flash chromatography using petroleum ether/ethyl acetate (8/2 followed by 65/35) as eluent to give 4-benzyloxy-3-methoxyacetophenone (30.3 g, 99%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087602B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-5361ab59f70448ae8738fc7abac188e4
출처 메모uspto-grants-2006_08