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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17894생성일: 2026년 10월 24일

Azobisisobutyronitrile → 6-bromomethyl-1-oxo-3-phenyl-1H-indene-2-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/17894

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물N-bromobutanimideHCID 67184—
반응물5-Methyl-3-oxo-1-phenylindene-2-carboxylic acid ethyl esterHCID 68699292—
촉매TungstenHCID 23964—
용매Carbon TetrachlorideHCID 5943—
생성물6-bromomethyl-1-oxo-3-phenyl-1H-indene-2-carboxylic acid ethyl esterHCID 6869754636.7%

반응 단계

6-Methyl-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (3 g, 10.3 mmol) was dissolved in carbon tetrachloride, and N-bromosuccinimide (2 g, 11.4 mmol) and 2,2′-azobisisobutyronitrile (500 mg, 3.09 mmol) were added thereto. Then, the mixture was refluxed for 3 hours under a 375 W tungsten lamp. After the reaction is completed, the organic layer was extracted with dichloromethane/saturated sodium chloride, dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain 6-bromomethyl-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (1.4 g, yield 36.7%) as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741323B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3886912e1cf84b7b8345cc647357f727
출처 메모uspto-grants-2010_06