Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hexane → 2-[2-(Benzenesulfonyl)-ethylsulfanyl]-3-nitropyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | 2-Chloro-3-nitropyridine | HCID 79613 | — |
| 반응물 | 2-(Phenylsulfonyl)ethanethiol | HCID 447093 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Sodium chloride; water | HCID 57417360 | — |
| 생성물 | 2-[2-(Benzenesulfonyl)-ethylsulfanyl]-3-nitropyridine | HCID 67133757 | 46% |
반응 단계
1.8 g (16.0 mmol) potassium tert-butylate were added to a solution of 3.0 g (14.8 mmol) 2-(phenylsulfonyl)ethanethiol in DMF (35 ml) and the mixture was stirred for 30 min at room temperature. Then 2.5 g (15.8 mmol) 2-chloro-3-nitropyridine were added and the mixture was stirred for a further 1 h at RT. Then it was diluted with a brine/EE mixture (1:1 vv) and stirred for a further 30 min at RT. Then the organic phase was separated off, washed with water and brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. Column chromatography (hexane/EE 6:1) of the residue yielded 2.2 g (6.8 mmol, 46%) 2-[2-(benzenesulfonyl)-ethylsulfanyl]-3-nitropyridine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08247573B2 |
| 출처 데이터셋 | uspto-grants-2012_08 |
| ORD ID | ord-6cd212b40b0f4f10b0d04144f712bace |
| 출처 메모 | uspto-grants-2012_08 |