
(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol synthesis
- Product Name:(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol
- CAS Number:302348-51-2
- Molecular formula:C13H19BO3
- Molecular Weight:234.1

128376-64-7
188 suppliers
$5.00/250mg

302348-51-2
133 suppliers
$5.00/250mg
Yield:302348-51-2 513 mg
Reaction Conditions:
with sodium tetrahydroborate at 20; for 5 h;
Steps:
[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanol (2a).
To a mixture of a4-formylbenzenboronic acid (1a, 375 mg, 2.50 mmol), pinacol (355 mg, 3.00 mmol) and anhydrous magnesium sulfate (625 mg, 5.00 mmol), methanol was added (12.50 mL). The mixture was stirred at room temperature for 6 h. After the reaction was completed, the crude solution was filtered, and then sodium borohydride (47 mg, 1.25 mmol) was added to the filtrate. Afterwards, the reaction mixture was stirred for an additional 5 h. Once the reaction was completed, the reaction mixture was filtered and the filtrate was concentrated in vacuo to give the desired product 2a as a white solid (m.p. 75-77 °C) in88% yield (513 mg). 1H-NMR (CD3OD-d4) δ ppm 7.71 (d, J = 8.0 Hz, 2H), 7.35 (d, J = 7.8 Hz, 2H),4.62 (s, 2H), 1.34 (s, 12H); 13C-NMR (CD3OD-d4) δ ppm 146.23, 135.93, 127.26, 85.19, 65.24, 25.34;11B-NMR (CDCl3) δ ppm 34.82.
References:
Chung, Sheng-Hsuan;Lin, Ting-Ju;Hu, Qian-Yu;Tsai, Chia-Hua;Pan, Po-Shen [Molecules,2013,vol. 18,# 10,p. 12346 - 12367]

873-75-6
313 suppliers
$6.00/5g

73183-34-3
585 suppliers
$6.00/5g

302348-51-2
133 suppliers
$5.00/250mg

18282-51-4
216 suppliers
$10.00/1g

73183-34-3
585 suppliers
$6.00/5g

302348-51-2
133 suppliers
$5.00/250mg

76-09-5
384 suppliers
$8.19/250mg

59016-93-2
327 suppliers
$5.00/1g

302348-51-2
133 suppliers
$5.00/250mg

873-76-7
344 suppliers
$6.00/10g

73183-34-3
585 suppliers
$6.00/5g

302348-51-2
133 suppliers
$5.00/250mg