HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5,5,6,6,6-pentafluorohexanenitrile → HCID 178470246, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5,5,6,6,6-pentafluorohexanenitrile | HCID 86679026 | — |
| Reactant | 2-Ethoxy-1-(methylsulfanyl)-2-oxoethaniminium tetrafluoroborate | HCID 86679027 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178470246 | HCID 178470246 | — |
Reaction Steps
A solution of 2-amino-5,5,6,6,6-pentafluorohexanenitrile (0.5722 g, 2.83 mmol) and 2-ethoxy-1-(methylsulfanyl)-2-oxoethaniminium tetrafluoroborate (0.808 g, 3.45 mmol) in dry 1,4-dioxane (5.2 mL) was stirred at 25° C. under N2 for 6 days. The solution was concentrated in vacuo. The resulting residue was purified by silica gel chromatography using DCM/MeOH gradient to afford the desired product, as an orange oil. 1H NMR (500 MHz, CHCl3-d): δ 4.36 (q, J=7.1 Hz, 2H); 2.85 (br s, 2H); 2.41-2.16 (m, 3H); 2.11-1.94 (m, 1H); 1.35 (t, J=7.1 Hz, 3H). m/z 302.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365574B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-88954e9615454032b714897fcf1c92ee |
| Source note | uspto-grants-2016_06 |