HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199247Generated: October 29, 2026
Ethyl trifluoroacetate → N-[1-[1-(6-Chloro-3-pyridyl)ethyl]-2-pyridylidene]-2,2,2-trifluoroacetamide
https://huagongshe.com/reaction/2199247
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-5-(chloromethyl)pyridine | HCID 155479 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[1-[1-(6-Chloro-3-pyridyl)ethyl]-2-pyridylidene]-2,2,2-trifluoroacetamide | HCID 14127920 | 81.2% |
Reaction Steps
In a mixture solvent of 30 mL of dimethylformamide and 20 ml of toluene, 9.4 g (0.1 mol) of 2-aminopyridine was dissolved, and 28.4 g (0.2 mol) of ethyl trifluoroacetate was added thereto, followed by stirring at 60 to 65° C. for 8 hours. To the reaction liquid, 16.6 g (0.12 mol) of potassium carbonate powder and 16.2 g (0.1 mol) of 2-chloro-5-chloromethylpyridine were added, followed by stirring at 60 to 65° C. for 15 hours. To the reaction liquid, 15 mL of methanol was added, and then the reaction liquid was added to 120 mL of hot water of 50° C. After being cooled to room temperature, the mixture was stirred for 2 hours. The crystals were filtered, and washed with 50 mL of water and 100 mL of toluene. The obtained crystals were dried under reduced pressure at 45° C. Thus, 25.6 g of the target compound was obtained (Percentage Yield: 81.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09357776B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-27fcaa1e47124c9b9c0e1d7f8961874f |
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| Source note | uspto-grants-2016_06 |
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