Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21965생성일: 2026년 10월 24일
Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate → Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate
https://huagongshe.com/ko/reaction/21965
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate | HCID 19930804 | — |
| 반응물 | HCID 178418680 | HCID 178418680 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate | HCID 19930812 | — |
반응 단계
Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (5.02 g, 20.81 mmol) is dissolved in ether (50 mL), and cooled to 0° C. Trimethylsilylmethylmagnesium chloride (42.0 mL of a 1.0M solution in ether, 42.0 mmol) is added dropwise, the reaction is stirred at 0° C. for 20 minutes, and then heated to reflux overnight. The reaction is quenched with saturated ammonium chloride, and extracted several times with ethyl acetate. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (10% ethyl acetate/hexane) to give separately the two diastereomers of ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate; major isomer, m.p. 129°-130° C.; minor isomer, m.p. 175°-177° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05426103 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-a31e8b575c884584a0ca2bedb89b6bf4 |
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| 출처 메모 | uspto-grants-1995_06 |
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