Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Methyl-5-hydroxypyridine → (S)-2-Methyl-5-oxiranylmethoxy-pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Methyl-5-hydroxypyridine | HCID 14275 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Benzenesulfonic acid, 3-nitro-, (2S)-2-oxiranylmethyl ester | HCID 146490 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (S)-2-Methyl-5-oxiranylmethoxy-pyridine | HCID 59686824 | — |
반응 단계
6-Methyl-pyridin-3-ol (0.218 g, 2.0 mmol) was placed in a flask with DMF (10 mL) and NaH (60% dispersion in oil, 77 mg, 2.0 mmol) and stirred for 30 min. at room temperature. (S)-glycidyl 3-nitrobenzene sulfonate (0.52 g, 2.0 mmol) was then added to the reaction mixture, which was then stirred at room temperature for 14 hours. The reaction was quenched with NaHCO3 (saturated) and then extracted three times with ethyl acetate. The organic layer was dried with magnesium sulfate, filtered and the solvent was evaporated under reduced pressure to yield crude product which was purified by silica gel chromatography (60% Ethyl acetate/heptane) to yield the title compound as a residue.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08530475B2 |
| 출처 데이터셋 | uspto-grants-2013_09 |
| ORD ID | ord-9bf078de8aa64806aabfd30258c40a4a |
| 출처 메모 | uspto-grants-2013_09 |