Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20525312 | HCID 20525312 | 52% |
Reaction Steps
A mixture of 27.0 g (0.50 mol) of sodium methoxide, 56.0 g (0.62 mol) of dimethyl carbonate, and 100 ml of dry tetrahydrofuran was agitated in a 350 ml tube under 1-3 atm of tetrafluoroethylene. Tetrafluoroethylene was pressured in as consumed until 110 g (1.1 mol) had been added. The mildly exothermic reaction kept the temperature near 35° C.; after the addition, the reaction mixture was heated at 40° C. for 1 hour. The viscous solution from this reaction was treated directly with 75.6 g (0.60 mol) of dimethyl sulfate at 40° C. for 15 hours. Filtration and distillation afforded 87.6 g (52%) of 1,2,2,5-tetramethoxyoctafluoropentane, bp 54° C. (0.3 mm Hg), nD24 1.3605, whose structure was confirmed by Ir 3.29, 3.33, and 3.42 (satd CH) 8-9μ (CF, COC). Nmr (CCl4) 'H δ 3.68 (s, 1, CF2OCH3) and 3.57 (p, JHF 1.3 Hz, 1, C (OCH3)2); 19F -88.2 (m, 1, CR2O) and -116.5 ppm (m, 1, CF 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04349650 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-0a5815be72a142f7beeab2e1c11183d8 |
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| Source note | uspto-grants-1982_09 |
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