2-(4-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane synthesis

12synthesis methods

Product Name:2-(4-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane
CAS Number:213596-33-9
Molecular formula:C12H17BO3
Molecular Weight:220.07

696-62-8
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$5.00/1g

126-30-7 Synthesis

126-30-7
601 suppliers
$8.00/100g

2-(4-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane

213596-33-9
29 suppliers
$79.00/1g

Yield:213596-33-9 99%

Reaction Conditions:

Stage #1:para-iodoanisole with diisopropopylaminoborane;triethylamine;triphenylphosphine;palladium dichloride in tetrahydrofuran at 65; for 12 h;Inert atmosphere;Alcaraz-Vaultier borylation;
Stage #2:2,2-Dimethyl-1,3-propanediol in tetrahydrofuran at 0 - 25; for 0.25 h;Inert atmosphere;Further stages;

Steps:

4.3. General procedure for the synthesis of an aryl boronic ester from the reaction of aryl iodides or bromides with BH₂N(ⁱPr)₂ in the presence of a palladium catalyst
General procedure: Triphenylphosphine (0.131 g, 0.5 mmol, 20 mol %), p-iodoanisol (0.585 g, 2.5 mmol), and triethylamine (1.78 mL, 12.5 mmol) were added to a 50 mL round-bottomed flask equipped with a sidearm, condenser, and stir bar. This solution was then degassed by alternating vacuum and argon three times. Palladium dichloride (0.023 g, 0.13 mmol, 5 mol %) was then added under positive argon pressure. After stirring at room temperature for 15 min diisopropylaminoborane (5 mL, 1 M THF, 5 mmol) was added and the reaction mixture was degassed again by alternating vacuum and argon three times. The reaction solution was then heated to reflux. After 12 h of reflux the reaction was cooled to 0 °C and neopentyl glycol (6 mL, 1 M solution in THF, 6 mmol) was slowly added through the condenser. After warming to 25 °C and stirring for 15 min. 1 M HCl (6 mL) was added and the mixture was filtered through a pad of Celite. The mixture was then extracted with diethyl ether (3×10 mL), combining all the organic fractions together. The organic fractions were then washed with a brine solution (2×10 mL), dried with magnesium sulfate and filtered. The solvent was removed under reduced pressure yielding 2-(4-methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane as a yellow oil.

References:

Haddenham, Dustin;Bailey, Christopher L.;Vu, Chau;Nepomuceno, Gabby;Eagon, Scott;Pasumansky, Lubov;Singaram, Bakthan [Tetrahedron,2011,vol. 67,# 3,p. 576 - 583] Location in patent:experimental part

5720-07-0 Synthesis