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HRID 238587作成日:2026年10月25日

Ethyl Bromide → Fluoresone

https://huagongshe.com/reaction/238587

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl BromideHCID 6332—
反応物4-Fluorobenzenesulfonyl chlorideHCID 9588—
反応物Sodium Phosphate, DibasicHCID 24203—
反応物Sodium SulfiteHCID 24437—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物FluoresoneHCID 7181463.2%

反応条件

温度60 °C

反応手順

To a solution of sodium hydrogen phosphate (14.2 g, 0.1 mol) and sodium sulfite (25.2 g, 0.2 mol) in water (200 mL) was added 4-fluoro-benzenesulfonyl chloride (19.5 g, 0.1 mol). After the mixture was stirred at 60° C. overnight, a solution of bromoethane (32.7 g, 0.3 mol) in acetone (20 mL) was added dropwise, followed by the addition of tetrabutylammonium iodide (3.7 g, 0.01 mol) in one portion. The resulting reaction mixture was stirred at room temperature for 5 days, then diluted with water (50 mL), and extracted with ethyl acetate (100 mL×3). The combined organic layers were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by flash column chromatography (elution with 20% ethyl acetate in petroleum ether) to afford 1-ethanesulfonyl-4-fluoro-benzene (11.9 g, 63%) as a yellow oil (reference: Arnold, Leggy A. A., et al., Org. Lett, 6 (2004), 3005-3007).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642629B2
出典データセットuspto-grants-2014_02
ORD IDord-7c0ad6e0853241309521ef6621b24da2
出典メモuspto-grants-2014_02