HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242001Generated: October 29, 2026
Ethyl 4,4,4-trifluoroacetoacetate → HCID 178516136, compound
https://huagongshe.com/reaction/2242001
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Reactant | 2-Chloro-5-fluoroaniline | HCID 2736509 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178516136 | HCID 178516136 | 51% |
Reaction Steps
A solution of ethyl 4,4,4-trifluoroacetoacetate (commercially available, 4 mL, 27.3 mmol, 1.05 eq.) in polyphosphoric acid (22 mL) was heated to 100° C. 2-chloro-5-fluoroaniline (3.78 g, 26.0 mmol, 1 eq.) was added slowly to the stirred hot solution. The resulting reaction mixture was further heated to 150° C. and then stirred at that temperature overnight (approximately 18 hours). The reaction was cooled to room temperature and water was added carefully. The resulting light brown precipitate was collected by vacuum filtration, washed with water and dissolved in ethyl acetate. The ethyl acetate solution was washed with brine, dried over anhydrous MgSO4 and concentrated on a rotary evaporator. The crude product was purified by flash chromatography on silica gel using hexane/ethyl acetate to give 3.54 g (51% yield) of the desired product as an off-white solid; MP=141-142; MS (ES) m/z (relative intensity): 266 (M+H)+ (100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07671056B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-e3ee1ae27c3f456392c90021689ebb8a |
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| Source note | uspto-grants-2010_03 |
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