HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979623Generated: November 1, 2026
Chlorotrifluoroethylene → 1,2,2-Trifluoroethenyl-triethylsilane
https://huagongshe.com/reaction/1979623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrifluoroethylene | HCID 6594 | — |
| Reactant | Chlorotriethylsilane | HCID 13819 | — |
| Reactant | Methanedione--ethanol (1/1) | HCID 19604758 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2,2-Trifluoroethenyl-triethylsilane | HCID 10921466 | 86.2% |
Reaction Steps
A reactor flushed with argon gas was cooled with a dry ice-ethanol cooling medium, and 2.03 g (0.0174 mol) of chlorotrifluoroethylene was introduced into the reactor. To this reactor, 17 ml of THF was introduced to bring the chlorotrifluoroethylene concentration to 1 mmol/ml, and then 2.35 g (0.016 mol) of chlorotriethylsilane was added. The reactor was cooled to -78° C., and 12 ml (0.018 mol) of butyllithium (1.47M hexane solution) was added in 1 hour. The mixture was stirred at 78° C. for 4 hours and at room temperature for about 1 hour. Workup was conducted in the same manner as in Example 1, whereby 2.64 g (86.2%) of triethyltrifluorovinylsilane was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04481366 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-416e37cab6ca48c594168148fdc0528c |
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| Source note | uspto-grants-1984_11 |
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