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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48129Erstellt: 25. Oktober 2026

Water → 2-Methanesulfonyloxyimino-4-p-tolyl-but-3-enenitrile

https://huagongshe.com/reaction/48129

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt2-Hydroxyimino-4-p-tolyl-but-3-enenitrileHCID 86759357—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Methanesulfonyloxyimino-4-p-tolyl-but-3-enenitrileHCID 5393625564,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

2-Hydroxyimino-4-p-tolyl-but-3-enenitrile (1.9 g; 0.01 mol) 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 (2.1 ml, 0.015 mol) dropwise over 20 min, keeping the temperature of the mixture below 5° C. The mixture is then stirred at 5-10° C. for 3.5 hours, 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 50 ml of ethanol yields 2-methanesulfonyloxyimino-4-p-tolyl-but-3-enenitrile (1.7 g; 64%) as off-white crystals, mp 134-135° C. with one part melting at 145° C. 1H-NMR reveals the presence of two isomers (probably E/Z around the imino double bond).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06703182B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-58d073c768784635b9455ee81640d83b
Quellennotizuspto-grants-2004_03