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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2755생성일: 2026년 10월 23일

Benzoyl Peroxide → 4-(Benzhydrylidene-amino)-3-bromomethyl-benzonitrile

https://huagongshe.com/ko/reaction/2755

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물4-(Benzhydrylidene-amino)-3-methyl-benzonitrileHCID 19350962—
용매Carbon TetrachlorideHCID 5943—
용매DichloromethaneHCID 6344—
생성물4-(Benzhydrylidene-amino)-3-bromomethyl-benzonitrileHCID 1049968656.9%

반응 단계

To a solution of 4-(benzhydrylidene-amino)-3-methyl-benzonitrile (1.36 g, 4.27 mmol) in 40 mL of CCl4 is added N-bromosuccinimide (0.84 g, 4.7 mmol) and benzoyl peroxide (0.22 g, 0.64 mmol). The solution is heated to reflux for 16 h. The solution is cooled to ambient temperatures. The solution is diluted with CH2Cl2. The solution is washed with 1N NaOH and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude material is purified by column chromatography eluting with a gradient of 5% EtOAc/hexanes to 10% EtOAc/hexanes. The title compound (0.91 g, 2.43 mmol) is obtained as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731315
출처 데이터셋uspto-grants-1998_03
ORD IDord-d5d7a05761ee49b4bed0ffdf724b4bc7
출처 메모uspto-grants-1998_03