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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26083생성일: 2026년 10월 23일

Benzyl Bromide → 2-(Benzyloxy)-1-bromo-4-(2-methyloctan-2-YL)benzene

https://huagongshe.com/ko/reaction/26083

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium hydrideHCID 82127—
반응물2-Bromo-5-(2-methyloctan-2-YL)phenolHCID 12788187—
용매DimethylformamideHCID 6228—
생성물2-(Benzyloxy)-1-bromo-4-(2-methyloctan-2-YL)benzeneHCID 12882164—

반응 단계

To a -18° C. slurry of 23.0 g. (0.575 mole) of potassium hydride in 400 ml. of N,N-dimethylformamide is added over a 45 minute period a solution of 150 g. (0.5 mole) of 2-(4-bromo-3-hydroxyphenyl)-2-methyloctane in 400 ml. of N,N-dimethylformamide (reaction temperature ≤ -15° C.). The reaction mixture is stirred 15 minutes longer after which a solution of 98.3 g. (0.575 mole) of benzyl bromide in 200 ml. of N,N-dimethylformamide is added. The mixture is then warmed to room temperature and stirred 30 minutes longer. It is quenched by addition to 6 liters of ice water. The quenched mixture is extracted six times with 500 ml. of ether. The combined extract is washed twice with one liter portions of water and once with one liter of saturated sodium chloride, dried over magnesium sulfate and evaporated to a quantitative yield of the title product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04147872
출처 데이터셋uspto-grants-1979_04
ORD IDord-b9ccb1c6746043d695dfe0015179ddd7
출처 메모uspto-grants-1979_04