Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178522125 | HCID 178522125 | 95.2% |
Reaction Steps
In 25 ml of N,N-dimethylformamide, 4.7 g (50 mmol) of 2-aminopyridine was dissolved, and 35.5 g (250 mmol) of ethyl trifluoroacetate was added thereto. After that, the mixture was stirred at 55 to 60° C. for 15 hours, and then 100 ml of ethyl acetate and 100 ml of water were added thereto. The resultant mixture was stirred, and then phase separation was conducted. The ethyl acetate layer was further washed with 100 ml of water and with 100 mL of aqueous sodium chloride, then dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Thus, 9.05 g of 2,2,2-trifluoro-N-(pyridin-2(1H)-ylidene)acetamide was obtained (95.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09357776B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-79fd52e4c5694112aa5117e15be4c90b |
|---|
| Source note | uspto-grants-2016_06 |
|---|