Boron trifluoride etherate, strictly boron trifluoride diethyl etherate, or boron trifluoride–ether complex, is the chemical compound with the formula BF3O(C2H5)2, often abbreviated BF3OEt2. It is a colorless liquid, although older samples can appear brown. The compound is used as a source of boron trifluoride in many chemical reactions that require a Lewis acid.[1] The compound features tetrahedral boron coordinated to a diethylether ligand.[2] Many analogues are known, including the methanol complex.
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Other names
Boron Trifluoride Ethyl Ether
Boron Trifluoride Diethyl Etherate | |
Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.003.355 |
PubChem CID
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UNII | |
UN number | 2604 |
CompTox Dashboard (EPA)
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Properties | |
C4H10BF3O | |
Molar mass | 141.93 g·mol−1 |
Appearance | colorless liquid |
Density | 1.15 g cm3 |
Melting point | −58 °C (−72 °F; 215 K) |
Boiling point | 126 °C (259 °F; 399 K) |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Flammable, Reacts with water, Corrosive |
GHS labelling: | |
Danger | |
NFPA 704 (fire diamond) | |
Flash point | 58.5 °C (137.3 °F; 331.6 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Reactions
editBoron trifluoride etherate serves as a source of boron trifluoride according to the equilibrium:
- BF3OEt2 BF3 + OEt2
The BF3 binds to even weak Lewis bases, inducing reactions of the resulting adducts with nucleophiles.[1]
References
edit- ^ a b Veronica Cornel; Carl J. Lovely (2007). "Boron Trifluoride Etherate". Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons. pp. rb249.pub2. doi:10.1002/047084289X.rb249.pub2. ISBN 978-0-471-93623-7.
- ^ V. V. Saraev; P. B. Kraikivskii; I. Svoboda; A. S. Kuzakov; R. F. Jordan (2008). "Synthesis, Molecular Structure, and EPR Analysis of the Three-Coordinate Ni(I) Complex [Ni(PPh3)3][BF4]". J. Phys. Chem. A. 112 (48): 12449–12455. Bibcode:2008JPCA..11212449S. doi:10.1021/jp802462x. PMID 18991433.