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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 655652생성일: 2026년 10월 23일

Cesium carbonate → 3-Methoxy-2-methoxymethoxy-5-(2-oxo-oxazolidin-3-yl)benzaldehyde

https://huagongshe.com/ko/reaction/655652

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-OxazolidinoneHCID 73949—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물5-Bromo-3-methoxy-2-(methoxymethoxy)benzaldehydeHCID 11565322—
촉매Tris(dibenzylideneacetone) dipalladiumHCID 9832798—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물3-Methoxy-2-methoxymethoxy-5-(2-oxo-oxazolidin-3-yl)benzaldehydeHCID 5748255349.4%

반응 조건

온도100 °C

반응 단계

2-oxazolidinone (0.38 g, 4.36 mmol), dipalladium tris(dibenzylideneacetone) (0.17 g, 0.18 mmol), 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (XANTPHOS)(0.32 g, 0.55 mmol) and cesium carbonate (1.66 g, 5.1 mmol) were added to a dioxane solution (20 ml) of 5-bromo-3-methoxy-2-methoxymethoxybenzaldehyde (1.0 g, 3.6 mmol) and the mixture was stirred at 100° C. for 24 hours under an argon atmosphere. The reaction solution was cooled to room temperature and ethyl acetate was added thereto. The mixture was filtrated by cerite. The filtrate was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate 4:1→1:1). The purified product was concentrated under reduced pressure. Ethyl acetate and diisopropyl ether were added to the residue. The insoluble matter thus purified was obtained by filtration and dried to obtain 3-methoxy-2-methoxymethoxy-5-(2-oxo-oxazolidin-3-yl)benzaldehyde (0.5 g) as white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071600B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-dae1f6bfb85a45d6a67fb97041da02c4
출처 메모uspto-grants-2011_12