Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethanethiol → 7-Hydroxy-4-methyl-3-pyridin-4-yl-chromen-2-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethanethiol | HCID 6343 | — |
| 반응물 | Aluminum bromide | HCID 24409 | — |
| 반응물 | 7-Methoxy-4-methyl-3-pyridin-4-yl-chromen-2-one | HCID 11659018 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 7-Hydroxy-4-methyl-3-pyridin-4-yl-chromen-2-one | HCID 135502913 | — |
반응 단계
To a solution of 7-methoxy-4-methyl-3-pyridin-4-yl-chromen-2-one (600 mg, 2.24 mmoL) in CH2Cl2 (10 mL) at 0° C. was added EtSH (˜1 mL) followed by AlBr3 (6.74 mmoL, 1.80 g). The mixture was slowly warm to room temperature and poured into ice sat. NaHCO3 solution. Extraction was conducted 3× with CH2Cl2. The combined organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated to give the crude material, which was then purified by silica gel column chromatography using hexanes:ethyl acetate 1:1 as eluent to afford the title product as pale yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07399767B2 |
| 출처 데이터셋 | uspto-grants-2008_07 |
| ORD ID | ord-2f8b5397725240e8bf29bd29c8541eb3 |
| 출처 메모 | uspto-grants-2008_07 |