Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54421생성일: 2026년 10월 24일
3,5-Dimethylisoxazole → 2-(3-Methyl-isoxazol-5-yl)-1-(2-tert.butyldimethylsiloxy-phenyl)-ethanone
https://huagongshe.com/ko/reaction/54421
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,5-Dimethylisoxazole | HCID 9312 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Methyl 2-tert.butyldimethylsiloxybenzoate | HCID 131719984 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 2-(3-Methyl-isoxazol-5-yl)-1-(2-tert.butyldimethylsiloxy-phenyl)-ethanone | HCID 131719983 | 50.4% |
반응 단계
52 ml of 1N solution of n-butyllithium in hexane were added to a solution of 6 g of 3,5-dimethylisoxazol in 200 ml of tetrahydrofuran at -78° C. After stirring for 1 h 15 g of methyl 2-tert.butyldimethylsiloxybenzoate in 50 ml of tetrahydrofuran were added at the same temperature. The reaction mixture was slowly warmed up to -20° C. A saturated aqueous solution of ammonium chloride was added, the mixture was extracted several times with ethylacetate. The organic phase was separated, washed with water and dried over magnesium sulfate. Chromatography on silica gel with heptane/ethylacetate gave 9.4 g of the product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05622953 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-a7602e0c89e6449eacff8936f61394cd |
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| 출처 메모 | uspto-grants-1997_04 |
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