HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979622Generated: October 31, 2026
Chlorotrifluoroethylene → 1,2,2-Trifluoroethenyl-triethylsilane
https://huagongshe.com/reaction/1979622
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrifluoroethylene | HCID 6594 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Chlorotriethylsilane | HCID 13819 | — |
| Reactant | Nitrogen pentane | HCID 131713955 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2,2-Trifluoroethenyl-triethylsilane | HCID 10921466 | 84.8% |
Reaction Steps
A reactor flushed with argon was cooled with a liquid nitrogen-pentane cooling medium, and 15.0 g (0.129 mol) of chlorotrifluoroetylene was fed into the reactor. To this reactor, 50 ml of anhydrous tetrahydrofuran (THF), 30 ml of diethyl ether (Et2O) and 30 ml of pentane were introduced to bring the concentration of chlorotrifluoroethylene to 1 mmol/ml. Then, 16.1 g (0.107 mol) of chlorotriethylsilane was introduced. The reactor was cooled to -130° C., and then 88 ml (0.140 mol) of a hexane solution of butyllithium (1.6M) was introduced over a period of one hour. Then, the temperature was gradually raised to room temperature over 7.5 hours. The reaction solution was filtered and dried through a column of Celite placed on anhydrous sodium sulfate. The solvent was removed, and the residue was distilled, whereby 17.8 g of triethyltrifluorovinylsilane was obtained as a colorless transparent oil (yield: 85.1%).
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-9917910f829e46d888517bdbeb80d796 |
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| Source note | uspto-grants-1984_11 |
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