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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1717513생성일: 2026년 10월 24일

Cesium carbonate → 5-Methoxy-2-(2-mesyloxyethoxy)-benzaldehyde

https://huagongshe.com/ko/reaction/1717513

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1,2-Ethanediol, 1,2-dimethanesulfonateHCID 20796—
반응물2-Hydroxy-5-methoxybenzaldehydeHCID 95695—
용매DimethylformamideHCID 6228—
생성물5-Methoxy-2-(2-mesyloxyethoxy)-benzaldehydeHCID 5976585578%

반응 조건

온도70 °C

반응 단계

To a vigorously stirred solution of 15,2 g (100 mmol) 2-hydroxy-5-methoxy-benzaldehyde and 42.4 g (130 mmol) caesium carbonate in 350 ml DMF at 0° C. was added 27,3 g (125 mmol) 1,2-bis-methanesulfonyloxy-ethane ((J. Med. Chem.; 47; 17; (2004); 4300-4315) in 50 ml DMF dropwisely. The reaction mixture was stirred vigorously at 70° C. for 5 h. The solvent was evaporated. 200 ml water and 200 ml ethyl acetate were added. The organic phase was separated. The aqueous phase was extracted three times with 100 ml ethyl acetate each. The combined organic phases were washed with 50 ml water and 50 ml brine. The organic phase was dried with magnesium sulfate and evaporated. The crude product was purified by silica column chromatography (gradient ethylacetate:hexane 1:6, ethyl acetate→1:2). The desired product 4a was obtained in 78% yield (21.4 g, 78 mmol) as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07803960B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-3d753c14c9994b67aa656b2412c7b636
출처 메모uspto-grants-2010_09