참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Trimethylsulfonium iodide | HCID 75127 | — |
| 반응물 | 3-Acetyl-6-methylpyridine | HCID 95292 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Methyl-5-(2-methyloxiran-2-yl)pyridine | HCID 59455255 | — |
반응 단계
DMSO is added to NaH (1-1.8 equiv.) and heated to 65° C. for 1 h. THF is added at the same temperature and heated for another 10 min. After 10 min., the reaction mixture is cooled to 0° C. Trimethylsulfonium iodide (1-1.2 equiv.) is added and the contents stirred for 10 min. after which the solution of 1-(6-methylpyridin-3-yl)ethanone (1 equiv.) in THF is added dropwise. After complete addition, the reaction mixture is stirred at RT for 2 h; the reaction is monitored by LCMS. After completion, the reaction mixture is poured in ice water, extracted in diethyl ether, dried over sodium sulfate and concentrated at 25° C. to get the crude product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08906925B2 |
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| 출처 데이터셋 | uspto-grants-2014_12 |
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| ORD ID | ord-6b52658adc9f4ce2b0cba25d94af68f6 |
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| 출처 메모 | uspto-grants-2014_12 |
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