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HRID 41780作成日:2026年10月24日

Water → 3-Bromocarbazole

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物CarbazoleHCID 6854—
反応物N-bromobutanimideHCID 67184—
溶媒Ether acetateHCID 21226428—
生成物3-BromocarbazoleHCID 25244676,989.703%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530672B2
出典データセットuspto-grants-2013_09
ORD IDord-45be7181a681439696cd651602c644a1
出典メモuspto-grants-2013_09