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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,5-Difluorophenylacetic acid | HCID 522823 | — |
| Reactant | Ethyl 2-oximinooxamate | HCID 9614369 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,5-Difluorophenylacetyl chloride | HCID 2758320 | — |
| Product | ethyl (2Z)-2-amino-2-[2-(2,5-difluorophenyl)acetyl]oxyiminoacetate | HCID 140579266 | 89.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618138B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-946d0e5a846645d1b74471c7724b6d9e |
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| Source note | uspto-grants-2013_12 |
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