HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653578Generated: October 30, 2026
Ethyl 3-amino-4,4,4-trifluorocrotonate → HCID 19023221, compound
https://huagongshe.com/reaction/653578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 3-amino-4,4,4-trifluorocrotonate | HCID 5702529 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 19889041 | HCID 19889041 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19023221 | HCID 19023221 | 8.7% |
Reaction Steps
1.10 g of ethyl 3-amino-4,4,4-trifluorocrotonate was added to a mixture of 0.33 g of sodium methoxide and 5 ml of dimethylformamide at room temperature. After standing for 20 minutes, the mixed solution was added with 1.76 g of 6-ethoxycarbonylamino-7-fluoro-3-oxo-4-propargyl-2H-1,4-benzoxazine and heated at 130° C. for 4 hours. After cooling the solution to room temperature, the solution was poured into ice water and the resultant solution was extracted twice with diethyl ether. The aqueous layer was made acidic with dilute hydrochloric acid and extracted three times with ethyl acetate. The ethyl acetate extract was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. After distilling off ethyl acetate, the residue was purified by column chromatography using chloroform as developing solvent to obtain 0.20 g of the objective compound as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05127935 |
|---|
| Source dataset | uspto-grants-1992_07 |
|---|
| ORD ID | ord-462e670f67d94c63bfb55c4e9c61cf65 |
|---|
| Source note | uspto-grants-1992_07 |
|---|