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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1625998생성일: 2026년 10월 27일

Benzyl Bromide → benzyl 5-bromo-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1625998

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물5-Bromo-1H-indole-2-carboxylic acidHCID 252137—
용매AcetonitrileHCID 6342—
생성물benzyl 5-bromo-1H-indole-2-carboxylateHCID 67077949—

반응 단계

Benzyl bromide (160 μl) and 1,8-diazabicyclo[5.4.0]undec-7-ene (201 μl) were added to a solution of 5-bromo-1H-indole-2-carboxylic acid (161 mg) in acetonitrile (3.5 ml) at room temperature, followed by stirring for 22.5 hours. The reaction solution was concentrated and separated by adding ethyl acetate and distilled water. The resulting organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The resulting residue was solidified from dichloromethane-hexane, collected by filtration and washed with hexane. This was dried under reduced pressure to give the title compound (189 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08785438B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-0681cde35a654fa7be887a086c549c18
출처 메모uspto-grants-2014_07