Triethyloxonium tetrafluoroborate
Structural formula | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
General | ||||||||||||||||
Surname | Triethyloxonium tetrafluoroborate | |||||||||||||||
other names |
Meerwein's reagent (ambiguous) |
|||||||||||||||
Molecular formula | (C 2 H 5 ) 3 O (BF 4 ) | |||||||||||||||
Brief description |
white solid |
|||||||||||||||
External identifiers / databases | ||||||||||||||||
|
||||||||||||||||
properties | ||||||||||||||||
Molar mass | 189.99 g mol −1 | |||||||||||||||
Physical state |
firmly |
|||||||||||||||
Melting point |
84-89 ° C |
|||||||||||||||
safety instructions | ||||||||||||||||
|
||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Triethyloxonium tetrafluoroborate is a chemical compound from the group of trialkyloxonium salts.
presentation
Triethyloxonium tetrafluoroborate can be obtained by reacting boron trifluoride diethyl etherate with epichlorohydrin .
properties
Triethyloxonium tetrafluoroborate is a white solid. It is available either as a solution in dichloromethane or stabilized with 1 to 5% diethyl ether .
use
Triethyloxonium tetrafluoroborate is a powerful ethylating agent . It can also be used to esterify acids and modify carboxyl residues in proteins.
Individual evidence
- ↑ a b c d e f data sheet Triethyloxonium tetrafluoroborate from Sigma-Aldrich , accessed on May 20, 2017 ( PDF ).
- ↑ data sheet Triethyloxonium tetrafluoroborate, 95%, stab. with 3-5% diethyl ether from AlfaAesar, accessed December 5, 2014 ( PDF )(JavaScript required) .
- ↑ H. Meerwein: TRIETHYLOXONIUM FLUOBORATE In: Organic Syntheses . 46, 1966, p. 113, doi : 10.15227 / orgsyn.046.0113 ; Coll. Vol. 5, 1973, p. 1080 ( PDF ).