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HRID 28265作成日:2026年10月25日

Phenethyl bromide → alpha-Phenethyl-2,4-dichlorobenzyl cyanide

https://huagongshe.com/reaction/28265

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethyl bromideHCID 7666—
反応物TetrahydrofuranHCID 8028—
反応物Sodium hydrideHCID 24758—
反応物2,4-DichlorophenylacetonitrileHCID 80566—
溶媒WaterHCID 962—
生成物alpha-Phenethyl-2,4-dichlorobenzyl cyanideHCID 12391165—

反応条件

温度30 °C

反応手順

Sodium hydride (0.13 mole as a 50% dispersion in mineral oil) is washed with 100 ml. of dry n-hexane to remove the mineral oil, then blanketed with dry nitrogen and suspended in 250 ml. of freshly distilled tetrahydrofuran. To this sodium hydride suspension is added dropwise at room temperature a solution of 2,4-dichlorobenzyl cyanide (25 g., 0.13 mole) dissolved in 100 ml. of tetrahydrofuran. When the addition is completed, the temperature is maintained at 30° C. for an additional 0.5 hours. A solution of phenethylbromide (26 g., 0.14 mole) is then added dropwise and the resultant reaction mixture is stirred at 40° C. overnight under nitrogen. The reaction mixture is poured into 1 liter of water and extracted with (3×200 ml.) of ether. The combined ether extracts are washed with water, dilute hydrochloric acid, saturated sodium bicarbonate solution, saturated sodium chloride solution and dried over magnesium sulfate. The solvent is evaporated and the crude product distilled (144°-56°/0.03 mm) to give 26.6 g. (70.5%) of product, which is identified by nmr.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04225723
出典データセットuspto-grants-1980_09
ORD IDord-c3178ad2e2c04db1a384f9147e3a6c47
出典メモuspto-grants-1980_09