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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-(4,6-Dimethoxy-2-pyrimidinyloxy)benzaldoxime | HCID 902198 | — |
| 반응물 | m-Chlorocinnamyl bromide | HCID 54032824 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Potassium Carbonate | HCID 11430 | — |
| 생성물 | O-(3-chlorocinnamyl)-2-(4,6-dimethoxy-2-pyrimidinyloxy)benzaldoxime | HCID 54274346 | 61.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04986846 |
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| 출처 데이터셋 | uspto-grants-1991_01 |
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| ORD ID | ord-1291390487a5469d85f51fce06c03e92 |
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| 출처 메모 | uspto-grants-1991_01 |
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