HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517707Generated: October 30, 2026
Triethylamine → 2-{[4-Cyano-3-(trifluoromethyl)phenyl]amino}-2-oxoethyl acetate
https://huagongshe.com/reaction/517707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetoxyacetyl chloride | HCID 26297 | — |
| Reactant | 4-Amino-2-(trifluoromethyl)benzonitrile | HCID 522170 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-{[4-Cyano-3-(trifluoromethyl)phenyl]amino}-2-oxoethyl acetate | HCID 66654709 | — |
Reaction Steps
To a stirred solution of 4-amino-2-(trifluoromethyl)benzonitrile (commercially available, for example from Maybridge, Cornwall, United Kingdom, 85.0 g) in DCM (1 liter) at 0° C. was added triethylamine (92.2 g, 0.913 mol) and the reaction stirred for 15 minutes. Then acetoxyacetylchloride (74.5 g, 0.547 mol) was added at 0° C. and the reaction stirred for 4 hours at room temperature. The reaction mixture was diluted with DCM and washed with ice water followed by aqueous NaHCO3. The organic layer was separated and washed with brine solution, dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude product was purified by triturating with diethyl ether (500 mL) to yield 2-{[4-cyano-3-(trifluoromethyl)phenyl]amino}-2-oxoethyl acetate (85.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115132B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-c86d9a811d044dab94ac0ad2502089e1 |
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| Source note | uspto-grants-2015_08 |
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