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HRID 1978672作成日:2026年10月24日

Sodium Iodide → 1-(4-Bromophenoxy)-2-methylthioethane

https://huagongshe.com/ja/reaction/1978672

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物4-BromophenolHCID 7808—
反応物2-Chloroethyl methyl sulfideHCID 10965—
反応物Potassium CarbonateHCID 11430—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-(4-Bromophenoxy)-2-methylthioethaneHCID 21995949—

反応条件

温度90 °C

反応手順

In DMF (120 ml) was dissolved 4-bromophenol (15 g). To the mixture was added at room temperature potassium carbonate (21.6 g) and then were added 2-chloroethylmethylsulfide (10 ml) and sodium iodide (15.6 g), and the mixture was stirred at 90° C. for 16 hours and cooled to room temperature. The reaction mixture was added to water, and the mixture was extracted with ethyl acetate, washed with saturated brine and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the residue was purified with silica gel column chromatography (hexane/ethyl acetate=8/1) to give 1-bromo-4-(2-methylthioethoxy)benzene (4.0 g). In THF (58 ml) was dissolved 1-bromo-4-(2-methylthioethoxy)benzene (3.9 g). To the mixture was added dropwise at −78° C. 1.6M n-butyllithium/hexane (10 ml), and the mixture was stirred for 1 hour. To the mixture was added dropwise a solution of trimethyl borate (4.6 g) in THF (9.3 ml), and the mixture was stirred for 30 minutes and warmed to room temperature. To the mixture was added 10% sulfuric acid (20 ml), and the mixture was stirred for 15 minutes. The reaction mixture was extracted with ethyl acetate, washed with saturated brine and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the residue was washed with hexane/isopropylether to give 4-(2-methylthioethoxy)phenyl borate (1.39 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06235771B1
出典データセットuspto-grants-2001_05
ORD IDord-87dca85b9f9a44558d0b16e7f1c7450f
出典メモuspto-grants-2001_05