Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → (3-Bromothien-2-yl) (3-methoxyphenyl)methanone oxime
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 반응물 | (3-Bromothien-2-yl) (3-methoxyphenyl)methanone | HCID 21915416 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | (3-Bromothien-2-yl) (3-methoxyphenyl)methanone oxime | HCID 72727313 | 87% |
반응 단계
Stir a mixture of (3-bromothiophen-2-yl)-(3-methoxyphenyl)methanone (7 g, 0.024 mol), hydroxylamine hydrochloride (3.09 g, 0.048 mol) and pyridine (40 mL) overnight at room temperature, and then heat the mixture (100° C.–105° C.) for four hours. TLC (dichloromethane) shows that the reaction is complete. Quench the reaction mixture with water and extract with ether (three times). Wash the ether phase with HCl (3N) and water, dry (MgSO4), filter and concentrate to yield an oil that solidifies. Recrystallize the solid from ether:hexane to obtain the title compound (6.4 g, 87% Yield), m.p. 102–103° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07125903B1 |
| 출처 데이터셋 | uspto-grants-2006_10 |
| ORD ID | ord-57b78ac06de9427ea6e74f79c1c384e6 |
| 출처 메모 | uspto-grants-2006_10 |