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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1359151생성일: 2026년 10월 25일

N-bromobutanimide → 6'-Methyl-2'-bromomethyl-2-(4-methoxybenzoyl)-biphenyl-4-carbonitrile

https://huagongshe.com/reaction/1359151

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물4'-Methoxy-2',6'-dimethyl-2-(4-methoxybenzoyl)-biphenyl-4-carbonitrileHCID 10894011—
반응물Nbs aibnHCID 86630000—
촉매AzobisisobutyronitrileHCID 6547—
용매Carbon TetrachlorideHCID 5943—
생성물6'-Methyl-2'-bromomethyl-2-(4-methoxybenzoyl)-biphenyl-4-carbonitrileHCID 1818274893.6%

반응 단계

To a refluxing solution of the compound from Step D (45.5 g, 122 mmol) and AIBN (1.0 g) in CCl4 (2.5 L) was added a mixture of NBS (23.0 g, 129 mmol) and AIBN (1.0 g) in ten equal portions. The reaction mixture was refluxed for 2 h after the addition of the last portion of NBS/AIBN. The reaction mixture was concentrated to approximately 1 L and washed 3 times with water (1 L). The organic layer was dried with anhydrous Na2SO4, filtered and the solvent removed. Toluene (200 ml) was added to the residue and then evaporated. Repeating this procedure gave 48 g of the title compound that was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06599921B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-3ec49c2663994f3995567c06e06a9d32
출처 메모uspto-grants-2003_07