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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48133Erstellt: 25. Oktober 2026

Water → 2-Methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile

https://huagongshe.com/reaction/48133

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt2-Hydroxyimino-4-(4-methoxy-phenyl)-but-3-enenitrileHCID 86759358—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrileHCID 5452275141%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

2-hydroxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile (1.8 g; 9 mmol) is dissolved in 15 ml of anhydrous tetrahydrofuran, and cooled to 0° C. Methanesulfonyl chloride (0.93 ml, 0.012 mol) is added at once, followed by triethylamine (2 ml, 0.015 mol) dropwise over 20 min, keeping the temperature of the mixture below 5° C. The mixture is then stirred at 2° C. for 1 h 15 min, and poured into 200 ml of iced water. The suspension is extracted with ethyl acetate, the organic extract is washed neutral with water, then with brine, and dried over magnesium sulfate. Rotary evaporation of the solvent and recrystallization from 80 ml of ethanol yields 2-methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile (1.02 g; 41%) as light yellow hair-like crystals, mp 147-152° C. (dec). 1H-NMR reveals the presence of only one isomer.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06703182B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-212d808d04a24f93b79c9b42fc64dcf5
Quellennotizuspto-grants-2004_03