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HRID 720019作成日:2026年10月26日

Tetrahydrofuran → 2-Bromo-9,9-dimethoxyethylfluorene

https://huagongshe.com/reaction/720019

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物2-Bromo-9H-fluoreneHCID 14336—
反応物2-Methoxyethyl methanesulfonateHCID 146293—
反応物Potassium tert-butoxideHCID 23665647—
溶媒WaterHCID 962—
生成物2-Bromo-9,9-dimethoxyethylfluoreneHCID 69587088—

反応手順

To a solution of 2-bromofluorene (2.45 g, 10 mmol) in tetrahydrofuran (dry, 75 ml) was added potassium t-butoxide (3.36 g, 30 mmol), giving a deep orange solution. The mixture was stirred at ambient temperature for 10 min and added 2-methoxyethyl mesylate in tetrahydrofuran dropwise. Exothermic reaction was observed. Stirring was continued at ambient temperature for overnight to give an orange solution. At the end of the reaction, it was diluted with water (150 ml). The products extracted with ethylacetate (30 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 (3.3 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-67040ca6b49542a6ac6a7c0f8ef870c1
出典メモuspto-grants-2006_11