참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 반응물 | 3-Bromo-2-chloro-6-methylpyridine | HCID 2734418 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 3-Bromo-2-chloro-6-methylpyridin-1-ium-1-olate | HCID 85706489 | 1,230.1% |
반응 단계
step a—To a solution of 3-bromo-2-chloro-6-methyl-pyridine (2.0 g, 0.687 mmol) in CHCl3 was added MCPBA (3.3 g, 19.1 mmol) and the resulting solution was heated at 50° C. overnight. The resulted solution was cooled and partitioned between DCM and sat'd. aq. NaHCO3. The organic layer was dried (Na2SO4), filtered and concentrated in vacuo. The crude product was purified by SiO2 chromatography eluting with an EtOAc/hexane gradient (30 to 80% EtOAc) to afford 1.88 g (87%) of 3-bromo-2-chloro-6-methyl-pyridine 1-oxide (357a) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08273773B2 |
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| 출처 데이터셋 | uspto-grants-2012_09 |
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| ORD ID | ord-018b7ca9aaaf4f3b845ebada39f7db3d |
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| 출처 메모 | uspto-grants-2012_09 |
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