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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704297생성일: 2026년 10월 25일

2-(4,6-Dimethoxy-2-pyrimidinyloxy)benzaldoxime → O-(3-chlorocinnamyl)-2-(4,6-dimethoxy-2-pyrimidinyloxy)benzaldoxime

https://huagongshe.com/reaction/704297

반응식

참여 물질

역할이름HCID투입량
반응물2-(4,6-Dimethoxy-2-pyrimidinyloxy)benzaldoximeHCID 902198—
반응물m-Chlorocinnamyl bromideHCID 54032824—
용매AcetoneHCID 180—
용매Potassium CarbonateHCID 11430—
생성물O-(3-chlorocinnamyl)-2-(4,6-dimethoxy-2-pyrimidinyloxy)benzaldoximeHCID 5427434661.5%

반응 단계

5.5 g of 2-(4,6-dimethoxy-2-pyrimidinyloxy)benzaldoxime and 4.6 g of 3-chlorocinnamyl bromide were dissolved in 30 ml of dry acetone containing 2.7 g of anhydrous potassium carbonate. The solution was heated for 5 hours under stirring and reflux. After the reaction mixture was allowed to cool down, the acetone was distilled out under reduced pressure and the resulting residue was dissolved in 200 ml of ethyl acetate. The ethyl acetate solution was washed with water and the organic layer was dried over anhydrous sodium sulfate. The solution was then concentrated under reduced pressure. The residue was purified by silica gel chromatography (developer: n-hexane:ethyl acetate: 4:1) to obtain 5.2 g of O-(3-chlorocinnamyl)-2-(4,6-dimethoxy-2-pyrimidinyloxy)benzaldoxime as a semi-solid substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04986846
출처 데이터셋uspto-grants-1991_01
ORD IDord-1291390487a5469d85f51fce06c03e92
출처 메모uspto-grants-1991_01