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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11201생성일: 2026년 10월 23일

Benzyl Bromide → 1-Bromo-4-phenylmethoxybenzene

https://huagongshe.com/ko/reaction/11201

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물4-BromophenolHCID 7808—
반응물Potassium CarbonateHCID 11430—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물1-Bromo-4-phenylmethoxybenzeneHCID 138835—

반응 단계

4-Bromophenol (2 g, 0.0116 mol) in acetone (40 ml) was treated with potassium carbonate (1.91 g, 1.2 equivalents) and benzyl bromide (1.44 ml, 1.05 equivalents). The reaction was refluxed under nitrogen. After 5–6 hours of reflux, the reaction was cooled to room temperature and diluted with an equal volume of ethyl acetate. This was diluted further with water and the organic layer was separated, dried over magnesium sulfate and evaporated to dryness to afford a white fluffy powder. Yield=2.36 g (73%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07097995B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-9c38a67482a74a60b22a9dd04f69b8a7
출처 메모uspto-grants-2006_08