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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1272222생성일: 2026년 10월 26일

Azobisisobutyronitrile → 3-(Bromomethyl)-1-benzothiophene

https://huagongshe.com/reaction/1272222

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물N-bromobutanimideHCID 67184—
반응물3-Methylbenzo[b]thiopheneHCID 73817—
용매Carbon TetrachlorideHCID 5943—
생성물3-(Bromomethyl)-1-benzothiopheneHCID 1126464142.2%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07208505B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-60dcc74147ce49ca9e0d702b0b0b53ad
출처 메모uspto-grants-2007_04