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HRID 720018作成日:2026年10月27日

Dimethylformamide → 2-Bromo-9,9-dimethoxyethylfluorene

https://huagongshe.com/reaction/720018

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物2-Bromo-9H-fluoreneHCID 14336—
反応物2-Bromoethyl methyl etherHCID 80972—
反応物Potassium tert-butoxideHCID 23665647—
溶媒WaterHCID 962—
生成物2-Bromo-9,9-dimethoxyethylfluoreneHCID 69587088—

反応条件

温度45 °C

反応手順

To a solution of 2-bromofluorene (2.0 g, 8.2 mmol) in dimethylformamide (dry, 30 ml) was added potassium t-butoxide (2.74 g, 24.4 mmol), giving a deep orange in color. The mixture was stirred at 45° C. for 20 min and added 2-bromoethylmethyl ether (3.5 g, 2.5 mmol) dropwise. Stirring was continued at the same temperature for overnight to give an orange solution. Another portion of 2-bromoethylmethyl ether (1.4 g, 1.0 mmol) was added and the mixture stirred at 80° C. for 4 h. It was diluted with water (100 ml). The products extracted with ethylacetate (20 ml) and washed with water. Organic layer was dried over magnesium sulfate and concentrated in vacuuo to afford the crude product. It was purified by preparative thin layer chromatography (silica gel, Rf=0.3 using hexane-EtOAc/3:2 as eluent) to give 2-bromo-9,9-dimethoxyethylfluorene (1.5 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07132572B2
出典データセットuspto-grants-2006_11
ORD IDord-dc989689314d4eefbdcd9bd4ab551516
出典メモuspto-grants-2006_11