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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23656생성일: 2026년 10월 24일

Sodium Hydroxide → 2-{3-[2-(2-Methoxyethoxy)ethoxy]phenyl}oxirane

https://huagongshe.com/ko/reaction/23656

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Trimethylsulfonium methyl sulfateHCID 2760871—
반응물3-[2-(2-Methoxyethoxy)ethoxy]benzaldehydeHCID 22574324—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
용매Sodium chloride; waterHCID 57417360—
생성물2-{3-[2-(2-Methoxyethoxy)ethoxy]phenyl}oxiraneHCID 22574382126.9%

반응 단계

To a stirred solution of 1.32 g of 3-[2-(2-methoxyethoxy)ethoxy]benzaldehyde and 15 mg of tetra-n-butylammonium bromide in 15 ml of CH2Cl2 is added a solution of 2.4 g of trimethylsulfonium methylsulfate in 4 ml of water, followed by 10 ml of 50% NaOH. The mixture is stirred and refluxed for 4 h, then cooled, diluted with ether and brine, and filtered. The organic phase is washed with brine, dried (MgSO4), and concentrated under reduced pressure to provide 1.78 g of the title compound as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852731B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-212bfc66156440dcb496d984dc7e2eed
출처 메모uspto-grants-2005_02