HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → 3,3,3-Trifluoro-1-nitropropene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 2,2,2-Trifluoro-1,1-ethanediol | HCID 67901 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,3,3-Trifluoro-1-nitropropene | HCID 220633 | 10% |
Reaction Steps
A mixture of 2,2,2-trifluoroethane-1,1-diol (75% aq solution, 20 g, 0.13 mol), CH3NO2 (24 g, 0.39 mol) and Na2CO3 (0.85 g, 8 mmol) was stirred overnight at RT. Water (50 mL) was added and the mixture was extracted with diethyl ether (3×30 mL) and dried over Na2SO4. After concentrating the organic extract at low temperature and under reduced pressure, P2O5 (20.0 g, 0.14 mol) was added to the residue oil, which was distilled at atmospheric pressure to give a green-yellow oil (4 g, 50% purity, 10% yield). Boiling point 85-90° C.; 1H NMR (400 MHz, CDCl3) δ ppm 7.09-7.17 (m, 1H), 7.50 (dd, J=2.0 Hz, 12.0 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08440689B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-77e29edd5ed64241b217010e92f51b99 |
| Source note | uspto-grants-2013_05 |