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HRID 47286作成日:2026年10月26日

Potassium Carbonate → 2-(5-Bromo-2-methoxy-phenylsulfanylmethyl)-benzonitrile

https://huagongshe.com/reaction/47286

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-(Bromomethyl)benzonitrileHCID 89599—
反応物5-Bromo-2-methoxybenzenethiolHCID 11276017—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-(5-Bromo-2-methoxy-phenylsulfanylmethyl)-benzonitrileHCID 2274485364.9%

反応条件

温度22 °C

反応手順

As depicted in Scheme 7 above, to a solution of 104 mg (0.470 mmol) of 2-methoxy-5-bromo-thiophenol in 5 mL of DMF was added 162 mg (1.18 mmol) of anhydrous to a solution of 104 mg (0.470 mol) of 2-methoxy-5-bromo-thiophenol in 5 mL of DMF was added 162 mg (1.18 mol) of anhydrous K2CO3. The solution was stirred for 15 minutes at 22° C. and 103 mg (0.520 mmol) of 2-bromomethyl-benzonitrile was added. The reaction was capped and heated to 40° C. for 12 hours. The mixture was subsequently diluted with 5 mL of water and extracted with ethyl acetate (2×10 mL). The organic extracts were washed with water (3×10 mL), brine (2×10 mL), and dried (Na2SO4). The solvent was evaporated and the product was purified on silica gel (eluting with 9:1 of hexane/ethyl acetate) to afford 102 mg of the product as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699873B1
出典データセットuspto-grants-2004_03
ORD IDord-4b3f9dc3e9d847e397c505f0fa752f86
出典メモuspto-grants-2004_03