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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253461생성일: 2026년 10월 26일

Dimethylformamide → 2-fluoro-5-methoxy-4-(1-methyl-1H-benzimidazol-2-ylmethoxy)-benzaldehyde

https://huagongshe.com/reaction/253461

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물4-(1H-benzimidazol-2-ylmethoxy)-2-fluoro-5-methoxy-benzaldehydeHCID 58086020—
생성물2-fluoro-5-methoxy-4-(1-methyl-1H-benzimidazol-2-ylmethoxy)-benzaldehydeHCID 5980387355%

반응 단계

4-(1H-Benzimidazol-2-ylmethoxy)-2-fluoro-5-methoxy-benzaldehyde (142) (0.600 g, 2.0 mmol) was dissolved in N,N-dimethylformamide (15 mL, 190 mmol). After the addition of sodium hydride (60% dispersion in oil, 0.072 g, 3.0 mmol) the reaction was stirred for 15 minutes at room temperature. Methyl iodide (140 μL, 2.2 mmol) was added dropwise to the mixture. The reaction was stirred overnight at room temperature under an atmosphere of nitrogen. The solvent was evaporated to dryness under reduced pressure. Ethyl acetate was added and the organic portion was washed with water, dried over anhydrous sodium sulfate and concentrated. Purification with silica gel flash chromatography with a gradient of ethyl acetate in hexanes gave the desired compound as a white powder (143, 0.345 g, 55%). MS (ESI) [M+H+]+=315.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872018B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-ed92e1fe79da49eaaf7820498ab0b543
출처 메모uspto-grants-2011_01