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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35080생성일: 2026년 10월 25일

Benzyl Bromide → 3-Benzyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione

https://huagongshe.com/reaction/35080

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물1-(4-Nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dioneHCID 14872629—
용매DimethylformamideHCID 6228—
생성물3-Benzyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dioneHCID 14872633—

반응 단계

4.92 g of 1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione are dissolved in 70 ml of dimethylformamide and, under a nitrogen atmosphere, 1.2 g of sodium hydride (pract. Fluka) are added. After stirring for 30 minutes at room temperature, the mixture is cooled to 0°, and a solution of 4.5 g of benzyl bromide in 10 ml of dimethylformamide is added dropwise thereto. After the addition is complete, the mixture is stirred at room temperature for 4 hours. The excess sodium hydride is destroyed by the addition of methanol, and concentration by evaporation is effected in vacuo. The residue is taken up in ethyl acetate and washed with water and aqueous sodium chloride solution. After drying over magnesium sulphate, the mixture is filtered and concentrated by evaporation. Melting point 150°-152° (from ether).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04764640
출처 데이터셋uspto-grants-1988_08
ORD IDord-c7da1d78a12a40c8a926c822e55f791f
출처 메모uspto-grants-1988_08