Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15130생성일: 2026년 10월 27일
Cesium fluoride → 1,1-Dimethylethyl [2-[1-(ethyloxy)ethenyl]-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate
https://huagongshe.com/reaction/15130
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium fluoride | HCID 25953 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| 반응물 | tert-Butyl (2-chloro-5-fluoro-6-methoxypyridin-3-yl)carbamate | HCID 71463986 | — |
| 촉매 | Bis(tri-tert-butylphosphine)palladium(0) | HCID 2734558 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 1,1-Dimethylethyl [2-[1-(ethyloxy)ethenyl]-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate | HCID 86614146 | — |
반응 단계
A degassed solution of 1,1-dimethylethyl [2-chloro-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate (20 g, 72.2 mmol) in 1,4-dioxane (200 ml) was treated with bis(tri-tert-butylphosphine) palladium(0) (1.05 g), caesium fluoride (21.93 g) and tributyl[1-(ethyloxy)ethenyl]stannane (26.9 ml) then heated to 100° C. overnight. The cooled mixture was treated with 10% aqueous potassium fluoride solution. After 0.5 hour stirring, the mixture was filtered through Kieselguhr, washing with 1,4-dioxane. Ethyl acetate and water were added to the filtrate. The phases were separated and the aqueous phase extracted twice with ethyl acetate. The combined organic extracts were dried over magnesium sulphate and evaporated. The residue was rapidly chromatographed eluting with 25-50% dichloromethane in hexane affording the product as a light brown oil (22.2 g, 99%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07732460B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-7f2d49d4ac4a426ea06dc7242d782435 |
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| 출처 메모 | uspto-grants-2010_06 |
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