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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16628생성일: 2026년 10월 23일

Benzyl Bromide → 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde

https://huagongshe.com/ko/reaction/16628

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물2-methyl-5-nitro-1H-indole-3-carbaldehydeHCID 609359—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehydeHCID 283825383.2%

반응 단계

To a solution of 2-methyl-5-nitro-1H-indole-3-carboxaldehyde (500 mg, 2.45 mmol) in DMF (5 ml) was added potassium carbonate (1.0 g, 7.35 mmol) and benzyl bromide (0.44 ml, 3.68 mmol). The mixture was stirred at room temperature for 4 h, diluted with EtOAc, washed with H2O, brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was triturated with Et2O-hexane to yield 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde (Compound 50) as a yellow solid (600 mg, 83%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737173B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-02e4b9ab0bf74da998fa4be994fe94f7
출처 메모uspto-grants-2010_06