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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979622Generated: October 31, 2026

Chlorotrifluoroethylene → 1,2,2-Trifluoroethenyl-triethylsilane

https://huagongshe.com/reaction/1979622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrifluoroethyleneHCID 6594—
ReactantHexaneHCID 8058—
ReactantChlorotriethylsilaneHCID 13819—
ReactantNitrogen pentaneHCID 131713955—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product1,2,2-Trifluoroethenyl-triethylsilaneHCID 1092146684.8%

Reaction Conditions

Temperature-130 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04481366
Source datasetuspto-grants-1984_11
ORD IDord-9917910f829e46d888517bdbeb80d796
Source noteuspto-grants-1984_11