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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1040403생성일: 2026년 10월 25일

Benzyl azide → 2-(1-benzyl-1H-1,2,3-triazol-4-yl)benzaldehyde

https://huagongshe.com/reaction/1040403

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl azideHCID 12152—
반응물2-EthynylbenzaldehydeHCID 640368—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(1-benzyl-1H-1,2,3-triazol-4-yl)benzaldehydeHCID 8665242065%
생성물2-(1-benzyl-1H-1,2,3-triazol-5-yl)benzaldehydeHCID 8665242130%

반응 단계

A solution of 2-ethynylbenzaldehyde (200 mg, 1.54 mmol) and benzyl azide (0.38 mL, 3.0 mmol) in 2.0 mL of N,N-dimethylformamide was stirred at 80° C. overnight. The reaction mixture was diluted with water, and the solution was extracted with a 5:1 solution (12 mL) of ethyl acetate and hexane. The extract was washed with water, brine, and dried over MgSO4. After filtration, the filtrate was concentrated in vacuo, and the residue was purified with silica gel column chromatography (hexane/ethyl acetate=80/20 to 60/40) to obtain 2-(1-benzyl-1H-1,2,3-triazol-4-yl)benzaldehyde (259 mg, 65%) and 2-(1-benzyl-1H-1,2,3-triazol-5-yl)benzaldehyde (118 mg, 30%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08552220B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-5f6252eb299946e0bd73a3877ad94ae8
출처 메모uspto-grants-2013_10