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HRID 247145作成日:2026年10月25日

Dimethylformamide → 2-(4-Bromophenyl)-2-methylpropanenitrile

https://huagongshe.com/reaction/247145

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物Benzeneacetonitrile, 4-bromo-HCID 27914—
溶媒WaterHCID 962—
生成物2-(4-Bromophenyl)-2-methylpropanenitrileHCID 1044359187.5%

反応手順

To a suspension of sodium hydride (60% dispersion in oil, 50 g, 1.25 m) in dry N,N-dimethylformamide (400 ml under nitrogen was added with stirring a solution of 4-bromophenylacetonitrile in N,N-dimethylformamide (400 ml) keeping the temperature between 30° and 40° C. A solution of iodomethane (213 g, 1.50 m) in N,N-dimethylformamide was then added gradually keeping the temperatue between 35° C. and the mixture then stirred at ambient temperature overnight. With ice cooling 2N aqueous hydrochloric acid (800 ml) was gradually added and then the mixture was diluted with water (1200 ml). The product was extracted with ether and the extract washed with water, saturated sodium bicarbonate, aqueous sodium sulphite, water again and finally brine. After drying and concentration on vacuo an orange oil was obtained which was distilled in vacuo to give the title compound as a colourless liquid (98.05 g, 87.5%) b.pt. 98°-100°/0.4 mm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04705854
出典データセットuspto-grants-1987_11
ORD IDord-871b5928d41841faa5759a279af95522
出典メモuspto-grants-1987_11