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HRID 397863作成日:2026年10月24日

Sodium Iodide → (2-(4-Bromophenoxy)ethyl)dimethylamine

https://huagongshe.com/ja/reaction/397863

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Potassium CarbonateHCID 11430—
反応物N,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物(2-(4-Bromophenoxy)ethyl)dimethylamineHCID 21387737.2%

反応条件

温度70 °C

反応手順

4-Bromophenol (10.0 g, 57.8 mmol) and 2-dimethylaminoethyl chloride hydrochloride (8.33 g, 57.8 mmol) were dissolved in DMF (200 ml), and potassium carbonate (24.0 g, 173 mmol) and sodium iodide (0.87 g, 5.78 mmol) were added under ice-cooling. The mixture was stirred for 13 hr at room temperature and at 70° C. for 3 hr. Water (400 ml) was added to the reaction mixture and the mixture was extracted with chloroform (2×200 ml). The organic layer was washed successively with water (2×200 ml) and saturated brine (200 ml), dried over anhydrous magnesium sulfate and concentrated. The obtained residue was dissolved in 1N hydrochloric acid (100 ml) and washed with ethyl acetate (2×200 ml). Sodium hydroxide (4 g) was added to the aqueous layer to make the layer alkaline, and the mixture was extracted with chloroform (2×200 ml). The organic layer was dried over anhydrous magnesium sulfate and concentrated. Hexane was added to the obtained residue and insoluble matter was filtered off. The mother liquor was concentrated to give the title compound (5.25 g, 37%) as a transparent oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610729B1
出典データセットuspto-grants-2003_08
ORD IDord-31029c0552b14ee298a96c2a93e10fee
出典メモuspto-grants-2003_08