Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Azobisisobutyronitrile → 3-(Bromomethyl)-1-benzothiophene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Azobisisobutyronitrile | HCID 6547 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | 3-Methylbenzo[b]thiophene | HCID 73817 | — |
| 용매 | Carbon Tetrachloride | HCID 5943 | — |
| 생성물 | 3-(Bromomethyl)-1-benzothiophene | HCID 11264641 | 42.2% |
반응 단계
3-Methylbenzo[b]thiophene (9.9 g, 67 mmol) is heated in carbon tetrachloride (133 ml ) to near reflux in the presence of n-bromosuccinimide (11.9 g, 67 mmol, 1.0 eq.). 2,2′Azobisisobutyronitrile (2.2 g, 13.3 mmol, 0.2 eq.) is added and the resulting mixture is refluxed for two hours. After cooling, the reaction mixture is filtered through a glass-fritted funnel, and the filtrate is concentrated. The residue is triturated with petroleum ether and toluene to afford 6.42 g of 3-Bromomethylbenzo[b]thiophene (42%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07087635B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-891086c3a8cc43c7beb58f68c0a282e1 |
| 출처 메모 | uspto-grants-2006_08 |