Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Thiophenol → 2-chloro-6-thiophenylpyridine N-oxide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Thiophenol | HCID 7969 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 2,6-Dichloropyridine N-Oxide | HCID 817673 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | 2-chloro-6-thiophenylpyridine N-oxide | HCID 86748730 | — |
반응 단계
The 1.64 g (0.010 moles) of 2,6-dichloropyridine N-oxide and 1.11 g (99%) (0.010 moles) of thiophenol was reacted with 0.400 g (0.010 moles) of ground sodium hydroxide of 16.4 ml of DMSO at 80° C. for 5 hours to give 2-chloro-6-thiophenylpyridine N-oxide. It was reacted with 1.20 g (0.030 moles) of ground sodium hydroxide at 80° C. for 2.5 hours to give 1-hydroxy-6-thiophenylpyridine-2-(1H)-one. After cooling, it was added 148 ml of water and was adjusted with 6N HCl to pH 3. The precipitate was filtered, washed with water and washed with hexanes to give 1.64 g (75%). It was recrystallized from ethanol: mp 180°-181° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05424435 |
| 출처 데이터셋 | uspto-grants-1995_06 |
| ORD ID | ord-dd733e1a9b8e43559d9f6fc67ca8840f |
| 출처 메모 | uspto-grants-1995_06 |