BrC₆F₅ (Fluorochem),
Mg turnings (Aldrich),
BF₃.Et₂O (Lancaster),
diethyl ether (dried over Na / benzophenone), toluene (dried over Na)

Suspend magnesium turnings (7.2 g, 0.3 mol) in diethyl ether (500 mL) at room temperature. Add BrC₆F₅ (74.1g, 0.3 mol) dropwise until the solution develops a grey turbid appearance. Cool the reaction on an ice bath and adjust the dropping rate to ensure that the solution does not reflux. Stir for an additional hour to ensure complete reaction. The resulting solution will be dark brown-black in appearance. Dissolve BF₃.Et₂O (0.1 mol, 14.19 g) in toluene (200 mL) and cool to 0 ºC. Add the Grignard reagent solution via a cannula with vigorous stirring. After addition allow the resulting solution to warm to room temperature. Remove approximately 500 mL of solvent under reduced pressure. Fit a reflux condenser and heat the solution to (almost) 100 ºC on a boiling water bath for one hour. During this time glassy solids will precipitate from solution. Remove all volatiles under vacuum until a dry brown cake is obtained (colourless crystals of B(C₆F₅)₃ may already be apparent). The product is isolated by extracting this cake with warm (45 ºC) hexanes (600 mL). As the hexane solution cools very fine feathery crystals will form. Cooling to -30 ºC will cause further crystallisation. The very fine nature of B(C₆F₅)₃ crystals obtained in this fashion makes them difficult to separate by filtration from the mother liquor. One solution is to add 30 mL of diethyl ether to the collection flask before filtration, now instead of obtaining feathery crystals of B(C₆F₅)₃, cubic crystals of (Et₂O)B(C₆F₅)₃ form, which can be easily separated by filtration. The yield depends upon the effort invested in the extraction process. We will typically extract the magnesium halides three times. For subsequent extractions we use the mother liquor obtained after crystallisation of the previous fraction. The best isolated yield obtained using this method was 70% Pure B(C₆F₅)₃ can be obtained from (Et₂O)B(C₆F₅)₃ or the crude product described above by sublimation (<0.1 mmHg, 100 ºC).

The preparation should be performed using standard Schlenk techniques. Cooling the Grignard reagent preparation minimises the extent to which the solution darkens, which we associate with decomposition, it also avoids the need to use a reflux condenser in what is a strongly exothermic reaction. It is necessary to remove the diethyl ether under reduced pressure before heating the reaction or sufficiently high reaction temperatures will not be obtained. The use of a boiling water bath is a device to obtain the optimum temperature. If the temperature is not high enough complete reaction will not occur and the product will be contaminated with (Et₂O)B(C₆F₅)₂F, which decomposes to give the oil B(C₆F₅)₂OEt during sublimation. If the reaction is heated above 100 ºC the yield is significantly reduced, presumably due to decomposition. B(C₆F₅)₃ is thermally stable but highly hygroscopic. We find it convenient to store samples long-term as the adduct, (Et₂O)B(C₆F₅)₃ and sublime as required.

Note: The ether adduct partially dissociates in CDCl₃ or C₆D₆ solution. The data presented here is for the ether-free material. ¹¹B NMR (293 K, d₆-benzene): 63 ¹⁹F NMR (293 K, d₆-benzene): -130 (o-F), -144 (p-F), -161 (m-F)

1. J. L. W. Pohlmann and F. E. Brinckman, Z. Naturforsch, 1965, 20b, 5.

2. A. G. Massey, A. J. Park and F. G. A. Stone, Proc. Chem. Soc., 1963, 212; A. G. Massey and A. J. Park, J. Organomet. Chem., 1964, 2, 245.