SODIUM TETRA(P-TOLYL)BORATE synthesis

8synthesis methods

Product Name:SODIUM TETRA(P-TOLYL)BORATE
CAS Number:15738-23-5
Molecular formula:B1C28H28Na1
Molecular Weight:398.32

13755-29-8 Synthesis

13755-29-8
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$6.00/25g

106-38-7
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$14.00/5g

15738-23-5
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$128.00/500mg

Yield:15738-23-5 96%

Reaction Conditions:

with magnesium in tetrahydrofuran at 0 - 20; for 12 h;Inert atmosphere;

Steps:

Sodium Tetra-4-tolylborate; Typical Procedure for the Synthesis ofSodium Tetraarylborates

Sodium tetraarylborates were prepared according to the literature, with some modifications. NaBF4 (1.0 g, 9.11 mmol) and Mg turnings(0.99 g, 41.00 mmol) were taken in an oven-dried sealed tube. The tube was filled with argon by the standard Schlenk technique. To this mixture, THF (20 mL) and 1,2-dibromoethane (40 μL, 0.46 mmol) were added, and the resulting mixture was stirred for 1 min. Finally,4-bromotoluene (4.7 mL, 38.3 mmol) was added in one shot at 0 °C. A very exothermic reaction started immediately after the addition of aryl halide. After the apparent exotherm had ceased, the resulting suspension was stirred at r.t. for 12 h. The solution became gray and white precipitates were formed. The reaction mixture was then added to aq Na2CO3. The resulting mixture was stirred for 30 min and then extracted with MeCN (3 × 30 mL). The combined organic layerwas washed with brine (50 mL), dried over MgSO4, filtered and concentratedunder reduced pressure with a rotary evaporator. The crude residue was purified by precipitation using Et2O-hexane (1:2) to provide sodium tetra-4-tolylborate as a white powder; yield: 3.48 g (8.75mmol, 96%).

References:

Osuka, Atsuhiro;Vasu, Dhananjayan;Yorimitsu, Hideki [Synthesis,2015,vol. 47,# 21,art. no. 47,p. 3286 - 3291]

13755-29-8 Synthesis

13755-29-8
460 suppliers
$6.00/25g

106-38-7
401 suppliers
$14.00/5g