HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → ETHYL 2-[(2,2,2-TRIFLUOROETHYL)AMINO]ACETATE(WXC09054)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Ethanamine, 2,2,2-trifluoro- | HCID 9773 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | ETHYL 2-[(2,2,2-TRIFLUOROETHYL)AMINO]ACETATE(WXC09054) | HCID 28596014 | — |
Reaction Steps
2,2,2-trifluoroethylamine (2.0 g) was added to a suspension of ethyl bromoacetate (2.3 mL), potassium iodide (0.34 g) in diisopropylethylamine (3.3 mL) and the mixture was stirred at RT for 5.5 h. The mixture was diluted with diethyl ether (30 mL), stirred at RT for 30 mins. The suspension was filtered and concentrated under reduced pressure. The sub-title compound (2.6 g) was obtained as a yellow oil; 1H NMR (300 MHz, CDCl3); 4.19 (2H, q), 3.50 (2H, s), 3.22 (2H, q), 1.26 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09376398B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-276800c65e9d44e18cc9eef479b31a66 |
| Source note | uspto-grants-2016_06 |