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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1072597생성일: 2026년 10월 27일

Azobisisobutyronitrile → 3-(Bromomethyl)-1-benzothiophene

https://huagongshe.com/reaction/1072597

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%). The title amine is prepared from 3-(bromomethyl)-benzo[B]thiophene in a similar fashion as described in U.S. Pat. No. 4,321,398.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06911463B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-72b57041208a4f0189159b5c6e89268c
출처 메모uspto-grants-2005_06