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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35283생성일: 2026년 10월 24일

Benzyl Bromide → 5-(Benzyloxy)-2-methoxybenzaldehyde

https://huagongshe.com/ko/reaction/35283

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Sodium HydroxideHCID 14798—
반응물5-Hydroxy-2-MethoxybenzaldehydeHCID 358341—
촉매Trioctylmethylammonium chlorideHCID 21218—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물5-(Benzyloxy)-2-methoxybenzaldehydeHCID 1096669491%

반응 단계

To a stirred suspension of 5-hydroxy-2-methoxybenzaldehyde (306.6 g, prepared by the method of Ulrich et al, J.Org.Chem., 1974, 39, 2437), benzyl bromide (355.8 g) and Adogen 464 (48.5 g) in dichloromethane (600 ml) was added a solution of sodium hydroxide (123.5 g) in water (500 ml). The mixture became warm and the suspension dissolved; additional dichloromethane (300 ml) was added to prevent crystallisation of the benzylated product. After 2 hours, the organic layer was removed, washed twice with water, once with saturated sodium chloride solution, then dried with anhydrous magnesium sulphate. The solution was concentrated, then treated with petroleum spirit to give 5-benzyloxy-2-methoxybenzaldehyde (445.7 g, 91%), m.p. 99°-100°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766121
출처 데이터셋uspto-grants-1988_08
ORD IDord-09acaa2b0fe944e185cdd2596e974e13
출처 메모uspto-grants-1988_08