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HRID 1697616作成日:2026年10月25日

1,2-Dibromoethane → 1-(2-Bromo-ethylsulfanyl)-2-trifluoromethyl-benzene

https://huagongshe.com/reaction/1697616

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DibromoethaneHCID 7839—
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物2-(Trifluoromethyl)benzenethiolHCID 2777889—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-(2-Bromo-ethylsulfanyl)-2-trifluoromethyl-benzeneHCID 66770769—

反応手順

To a stirred solution of 2-(trifluoromethyl)thiophenol (2.96 ml, 22 mmol; CAS Reg. No. 13333-97-6) in DMF (65 ml) were added 1,2-dibromoethane (9.67 ml, 112 mmol) and potassium carbonate (3.41 g, 25 mmol). The reaction mixture was stirred for 2 h 30 min at ambient temperature. AcOEt (30 ml) and water (30 ml) were added and the layers were separated. The aqueous layer was extracted three times with AcOEt (3×20 ml). The combined organic layers were washed with brine, dried over sodium sulfate and filtered. The solvent was removed under reduced pressure to give the title compound as yellow oil (6.0 g, 22 mmol; quant.) which was sufficiently pure to be used in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08163793B2
出典データセットuspto-grants-2012_04
ORD IDord-3e39a79ec8c34e3f8ddb3a5b6f312470
出典メモuspto-grants-2012_04