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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 421529생성일: 2026년 10월 26일

N-bromobutanimide → 3-Bromo-9-phenylcarbazole

https://huagongshe.com/reaction/421529

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물9-PhenylcarbazoleHCID 70851—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물3-Bromo-9-phenylcarbazoleHCID 1894262488.1%

반응 단계

Into a 2 L Meyer flask was put 24.3 g (100 mmol) of 9-phenylcarbazole, and dissolved in 600 mL of glacial acetic acid. Then, 17.8 g (100 mmol) of N-bromosuccinimide was slowly added thereto, followed by stirring at room temperature for about 12 hours. This glacial acetic acid solution was dropped into 1 L of ice water while being stirred. A white solid substance was precipitated and collected by suction filtration, and then the white solid substance was washed with water three times while being suction filtered. This solid substance was dissolved in 150 mL of diethyl ether, and this solution was washed with a saturated aqueous solution of sodium hydrogen carbonate and water. The resulting organic layer was dried with magnesium sulfate. This mixture was suction filtered, and the obtained filtrate was concentrated to give an oily substance. This oily substance was dissolved in about 50 mL of methanol. The resulting solution was left still to precipitate a white solid. This solid substance was collected by suction filtration and dried. Then, 28.4 g (88% yield) of 3-bromo-9-phenylcarbazole was obtained as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101289B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-17097e6a68924dc2bb7e1a656ee12d22
출처 메모uspto-grants-2012_01