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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46102생성일: 2026년 10월 23일

Benzyl Bromide → (1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-ol

https://huagongshe.com/ko/reaction/46102

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물TetrahydrofuranHCID 8028—
반응물Sodium HydroxideHCID 14798—
반응물15-Crown-5HCID 36336—
반응물(1R,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diolHCID 9989289—
생성물(1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-olHCID 10036335—

반응 조건

온도10 °C

반응 단계

To a stirred solution of (1R,2S,4R,5S)-bicyclo[2.2.1]-heptane-2,5-diol (1.15 g, 8.97 mmol) and 15-crown-5 (0.054 mL, 0.269 mmol) in tetrahydrofuran (30.0 mL, 8.97 mmol) were added at 10° C. (ice/water bath) finely ground sodium hydroxide (2.15 g, 53.8 mmol) and 1-(bromomethyl)benzene (1.07 mL, 8.97 mmol). After stirring at 10° C. for 3 h, the mixture was stirred at ambient temperature overnight. The mixture was partitioned between EtOAc and water, and the organic portions were washed with brine, and conc. in vacuo. The crude product was purified by flash column chromatography (0 to 80% of ethyl acetate in hexanes). The title compound was obtained as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541592B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-0398e47c3d9a4f728465e8b40c186dab
출처 메모uspto-grants-2013_09