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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41780생성일: 2026년 10월 23일

Water → 3-Bromocarbazole

https://huagongshe.com/ko/reaction/41780

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물CarbazoleHCID 6854—
반응물N-bromobutanimideHCID 67184—
용매Ether acetateHCID 21226428—
생성물3-BromocarbazoleHCID 25244676,989.703%

반응 단계

32 g (0.19 mmol) of 9H-carbazole was put into a 2 L Erlenmeyer flask, and then ether acetate (1.2 L) was added thereto so that the 9H-carbazole was dissolved in the ether acetate. To this solution was added 34 g (0.19 mol) of N-bromosuccinimide (NBS), and the mixture was stirred for about 15 hours in the air at room temperature. After the stirring, water was added to the mixture so that the precipitate was dissolved in the mixture. The organic layer of this mixture was washed with water three times and then with a saturated saline solution once. Magnesium sulfate was added so that the organic layer was dried. After the drying, the mixture was subjected to gravity filtration. The obtained filtrate was condensed to give a white solid. The obtained solid was recrystallized with ether acetate/hexane to give 36 g of a white powdered solid, which was the object of the synthesis, at a yield of 67%. A synthesis scheme of Step 1 is shown in (c-1) given below.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530672B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-45be7181a681439696cd651602c644a1
출처 메모uspto-grants-2013_09