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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20535생성일: 2026년 10월 23일

Benzyl Bromide → Methyl 3-(benzyloxy)-5-hydroxybenzoate

https://huagongshe.com/ko/reaction/20535

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물Methyl 3,5-DihydroxybenzoateHCID 75076—
용매DimethylformamideHCID 6228—
생성물Methyl 3-(benzyloxy)-5-hydroxybenzoateHCID 747202821%

반응 단계

To a stirred solution of methyl 3,5-dihydroxybenzoate (5.95 mol) in DMF (6 L) was added potassium carbonate (9 mol), and the suspension stirred at ambient temperature under argon. To this was added benzyl bromide (8.42 mol) slowly over 1 hour, with a slight exotherm, and the reaction mixture stirred overnight at ambient temperature. The reaction was quenched cautiously with ammonium chloride solution (5 L) followed by water (35 L). The aqueous suspension was extracted with DCM (1×3 L and 2×5 L). The combined extracts were washed with water (10 L) and dried overnight (MgSO4). The solution was evaporated in vacuo, and the crude product chromatographed in 3 batches (flash column, 3×2 kg silica, eluting with a gradient consisting of hexane containing 10% DCM, to neat DCM, to DCM containing 50% ethyl acetate) to eliminate starting material. The crude eluant was further chromatographed in 175 g batches (Amicon HPLC, 5 kg normal-phase silica, eluting with isohexane containing 20% v/v of ethyl acetate) to give the desired compound (21% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745475B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1ee42e706aa146c481c885bce5e2b5fa
출처 메모uspto-grants-2010_06