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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 612358Erstellt: 25. Oktober 2026

Water → (5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile

https://huagongshe.com/reaction/612358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt(5-Hydroxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrileHCID 59115159—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrileHCID 5444199477,2%

Reaktionsschritte

5 g (22 mmol) of (5-Hydroxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile are dissolved in 50 ml of THF and cooled in an ice bath. After adding 4.6 ml (33 mmol) of triethylamine to the solution, 1.9 ml (24 mmol) of methanesulfonyl chloride are added dropwise, keeping the temperature below 5° C. The reaction mixture is stirred while cooling in an ice bath for 30 min. The reaction mixture is poured into 200 ml of water, and extracted with ethyl acetate. The organic phase is washed with hydrochloric acid solution and sodium chloride solution. The organic phase is dried over MgSO4, the solvent is distilled off, and the residue is purified by recrystallization from toluene. 5.2 g (77%) of (5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile are obtained in the form of greenish brown crystals having a melting point of 160-162° C. (dec.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06004724
Quelldatensatzuspto-grants-1999_12
ORD IDord-607654a676584d24bb1028defa5a2427
Quellennotizuspto-grants-1999_12