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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918560Generated: October 26, 2026

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

https://huagongshe.com/reaction/1918560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,5-Difluorophenylacetic acidHCID 522823—
ReactantEthyl 2-oximinooxamateHCID 9614369—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product2,5-Difluorophenylacetyl chlorideHCID 2758320—
Productethyl (2Z)-2-amino-2-[2-(2,5-difluorophenyl)acetyl]oxyiminoacetateHCID 14057926689.3%

Reaction Conditions

Temperature-10 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-946d0e5a846645d1b74471c7724b6d9e
Source noteuspto-grants-2013_12