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HRID 2305759作成日:2026年10月26日

Dimethyl Sulfoxide → 3,3-Bis-methylthio-2-(2,5-dimethylbenzoyl)-acrylonitrile

https://huagongshe.com/reaction/2305759

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Methyl iodideHCID 6328—
反応物Carbon DisulfideHCID 6348—
反応物Sodium hydrideHCID 24758—
反応物2,5-DimethylbenzoylacetonitrileHCID 15895264—
溶媒WaterHCID 962—
生成物3,3-Bis-methylthio-2-(2,5-dimethylbenzoyl)-acrylonitrileHCID 15895265—

反応条件

温度18 °C

反応手順

A solution of 4.96 g (28.6 mmol) of 2-cyano-2′,5′-dimethylacetophenone in 120 mL of dry dimethyl sulfoxide and 3.43 mL (57.3 mmol) of carbon disulfide in a flame-dried 3-neck round bottom flask under dry nitrogen was stirred at 15-18° C. while 1.41 g (58.7 mmol) of oil free sodium hydride was added in 5 portions. The resulting deep red solution was stirred for 1 hour at 18° C. and then cooled to 15° C. whereupon 3.92 mL (8.95 g, 63.0 mmol) of methyl iodide was added dropwise. The temperature rose to about 22° C. during the addition. After stirring for 2 hours at room temperature, the reaction mixture was poured into cold water and the aqueous layer was extracted three times with ethyl acetate. The combined extracts were washed three times with water and then dried with brine and magnesium sulfate. Evaporation gave 8.96 g of the title compound as a heavy orange oil which crystallized in the refrigerator. The analytical sample crystallized from ethanol, m.p. 74.5-75.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06441018B2
出典データセットuspto-grants-2002_08
ORD IDord-f278680c5728453a8f888920e34d373f
出典メモuspto-grants-2002_08