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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2167835생성일: 2026년 10월 27일

Benzyl Bromide → Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-

https://huagongshe.com/reaction/2167835

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물4'-Hydroxy-3'-methylacetophenoneHCID 70135—
용매AcetoneHCID 180—
생성물Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-HCID 1296932599.1%

반응 단계

A mixture of 4′-hydroxy-3′-methylacetophenone (10.00 g; 66.6 mmol) and K2CO3 (13.80 g; 99.9 mmol) in acetone (100 mL) was stirred, at RT for 40 minutes. Subsequently, benzyl bromide (7.9 mL; 66.6 mmol) was added and the resulting mixture was heated under reflux for 2.5 h. After cooling to RT the mixture was concentrated in vacuo. The residue was dissolved in EtOAc, washed with 5% aqueous ammonia, water, and brine, dried (MgSO4), filtered and concentrated in vacuo to afford 1-(4-benzyloxy-3-methylphenyl)-ethanone (15.86 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09045441B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-eee07cea7e334acc82d58ad89ec6569c
출처 메모uspto-grants-2015_06