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HRID 58573Erstellt: 25. Oktober 2026

Thionyl Chloride → ethyl (2Z)-2-amino-2-[2-(2,5-difluorophenyl)acetyl]oxyiminoacetate

https://huagongshe.com/reaction/58573

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
EduktDiisopropylethylamineHCID 81531—
Edukt2,5-Difluorophenylacetic acidHCID 522823—
EduktEthyl 2-oximinooxamateHCID 9614369—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,5-Difluorophenylacetyl chlorideHCID 2758320—
Produktethyl (2Z)-2-amino-2-[2-(2,5-difluorophenyl)acetyl]oxyiminoacetateHCID 14057926689,3%

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

2-(2,5-difluorophenyl)acetyl chloride was prepared by heating overnight a suspension of 2,5-difluorophenylacetic acid (0.865 g; 3.67 mmol) and thionyl chloride (1.34 mL; 18.15 mmol) in chloroform (30 mL) at 80° C. After evaporation of the solvent and the excess of the thionyl chloride under reduced pressure, the residue was dissolved in dried dichloromethane (10 mL). This solution was added to a suspension of (Z)-ethyl 2-amino-2-(hydroxyimino)acetate (0.500 g; 3.67 mmol) and N,N-diisopropylethylamine (1.03 mL; 5.87 mmol) in dry dichloromethane (20 mL) cooled at −10° C. and stirred for 10 minutes. The mixture was stirred at room temperature for 23 h and poured into a mixture of ice/water. The white precipitate is filtered off and washed with dichloromethane and dried under reduced pressure to afford 0.469 g (45%) of (Z)-ethyl 2-amino-2-(2-(2,5-difluorophenyl)acetoxyimino)acetate as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434722B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-df82a9a4b29f464b8ae2c3b93118fae7
Quellennotizuspto-grants-2016_09