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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19987생성일: 2026년 10월 24일

Benzyl Bromide → 2-(Benzyloxy)-1-methoxy-4-nitrobenzene

https://huagongshe.com/ko/reaction/19987

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물2-Methoxy-5-nitrophenolHCID 69471—
용매AcetoneHCID 180—
생성물2-(Benzyloxy)-1-methoxy-4-nitrobenzeneHCID 531403696.5%

반응 단계

Potassium carbonate (1.65 gm; 12 mmol) was added to a solution of 2-methoxy-5-nitro phenol (1.69 g; 10 mmol) and benzyl bromide (1.71 gm; 10 mmol) in acetone (60 ml). The reaction mixture was refluxed for 12 hours. The solvent was removed under reduced pressure and the residue was partitioned between ethyl acetate (150 ml) and water (50 ml). The ethyl acetate layer was separated, washed with water (2×50 ml), dried over anhydrous magnesium sulfate. Removal of the solvent under reduced pressure provided 2.5 g of 1-Benzyloxy-2-methoxy-5-nitrobenzene (Yield=96.5%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745490B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-dfb5a266abc740b7aeafad57481660b5
출처 메모uspto-grants-2010_06