Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 526709생성일: 2026년 10월 24일
Diethyl Oxalate → Lithium 3-ethoxycarbonyl-2-methyl-3-oxo-1-(4-trifluoromethyl-phenyl)-propan-1-olate
https://huagongshe.com/ko/reaction/526709
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Oxalate | HCID 7268 | — |
| 반응물 | p-Trifluoromethylpropiophenone | HCID 136554 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 용매 | Methylcyclohexane | HCID 7962 | — |
| 생성물 | Lithium 3-ethoxycarbonyl-2-methyl-3-oxo-1-(4-trifluoromethyl-phenyl)-propan-1-olate | HCID 89907367 | — |
반응 단계
To a solution of 118 ml of lithium bis(trimethylsilyl)amide (Lithium Hexamethyldisilazide; 0.9 M in methylcyclohexane) was added dropwise over 15 min 20 g of 1-(4-Trifluoromethyl-phenyl)-propan-1-one in 51 ml methylcyclohexane at while maintaining the reaction mixture at 15-25° C. After stirring for 2 h, 15 ml of diethyl oxalate were added dropwise over 30 min and the reaction mixture was stirred for 16 h. Then, the precipitated product was collected by filtration and washed with n-heptane. The isolated crude product was used in the next reaction step after drying in vacuo. Yield: 19 g.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09346762B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-279f4601fcee4807b53a4ee69d049440 |
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| 출처 메모 | uspto-grants-2016_05 |
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