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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1279274Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1279274

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktMethyl iodideHCID 6328—
EduktCarbon DisulfideHCID 6348—
EduktSodium hydrideHCID 24758—
Edukt2,5-DimethylbenzoylacetonitrileHCID 15895264—
LösungsmittelWaterHCID 962—
Produkt3,3-Bis-methylthio-2-(2,5-dimethylbenzoyl)-acrylonitrileHCID 15895265—

Reaktionsbedingungen

Temperatur18 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06448265B1
Quelldatensatzuspto-grants-2002_09
ORD IDord-6b8076c7c034418a9fc9d8c133109b0c
Quellennotizuspto-grants-2002_09