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HRID 29246생성일: 2026년 10월 24일

Azobisisobutyronitrile → (6-Bromo-3-bromomethyl-benzofuran-2-yl)(2,4-dichlorophenyl)-methanone

https://huagongshe.com/ko/reaction/29246

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물N-bromobutanimideHCID 67184—
반응물(6-Bromo-3-methyl-benzofuran-2-yl)(2,4-dichloro-phenyl)methanoneHCID 59788907—
용매Carbon TetrachlorideHCID 5943—
생성물(6-Bromo-3-bromomethyl-benzofuran-2-yl)(2,4-dichlorophenyl)-methanoneHCID 5978888878.9%

반응 단계

To a solution of (6-bromo-3-methyl-benzofuran-2-yl)-(2,4-dichloro-phenyl)-methanone (3.0 g, 7.81 mmol) in carbon tetrachloride (30 mL) was added N-bromosuccinimide (1.46 g, 8.2 mmol) and 2,2′-azobisisobutyronitrile (128 mg, 0.78 mmol). The reaction mixture was refluxed for 6 h, then filtered. The filtrate was concentrated and the crude product was triturated with 10% EtOAc/hexane to afford the desired product as a pale yellow solid (2.85 g, 78.9%). This material was used in the subsequent step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420066B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-e72283bc9ddc4e078eb8f910a1eef417
출처 메모uspto-grants-2008_09