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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 325831Erstellt: 24. Oktober 2026

Dimethyl Sulfoxide → 2-[5-(2-Cyano-4-fluorophenoxy)-2-methylthiophenoxy]propionamide

https://huagongshe.com/de/reaction/325831

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktWaterHCID 962—
Edukt2-BromopropanamideHCID 101118—
Edukt5-(2-Cyano-4-fluorophenoxy) 2-(methylthio)phenolHCID 20462849—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produkt2-[5-(2-Cyano-4-fluorophenoxy)-2-methylthiophenoxy]propionamideHCID 131713486—

Reaktionsschritte

5-(2-Cyano-4-fluorophenoxy)-2-(methylthio)phenol (0.05 mole) potassium carbonate (0.2 mole), 2-bromopropionamide (0.08 mole) and dimethylsulfoxide (200 ml) are charged into a 500 ml glass reaction flask equipped with a mechanical stirrer. The reaction mixture is stirred at room temperature for a period of about 8 hours. After this time the mixture is poured into 500 ml of water. The resulting mixture is extracted three times with 100 ml portions of methylene chloride. The extracts are then combined, washed with water and thereafter dried. The dried solution is then stripped of solvent under reduced pressure to leave a residue. The residue is subjected to chromatography using a clay column and hexane/ethyl acetate mixtures as the eluant. The fractions containing the product are combined and stripped of solvent to yield the desired product 2-[5-(2-cyano-4-fluorophenoxy)-2-methylthiophenoxy]propionamide as the residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04443248
Quelldatensatzuspto-grants-1984_04
ORD IDord-558b3d313b6544dda8e9439e419a4d5b
Quellennotizuspto-grants-1984_04