Basic information Safety Supplier Related

3-Hydroxy-2,3-diMethylbutan-2-yl hydrogen (2,6-diMethylpyridin-3-yl)boronate

Basic information Safety Supplier Related

3-Hydroxy-2,3-diMethylbutan-2-yl hydrogen (2,6-diMethylpyridin-3-yl)boronate Basic information

Product Name:
3-Hydroxy-2,3-diMethylbutan-2-yl hydrogen (2,6-diMethylpyridin-3-yl)boronate
Synonyms:
  • 3-Hydroxy-2,3-diMethylbutan-2-yl hydrogen (2,6-diMethylpyridin-3-yl)boronate
  • 2,6-DiMethylpyridine-3-boronic acid pinacol ester
  • 2,6-Dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2,6-Dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)
  • Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxabor...
  • (2,6-Dimethylpyridin-3-yl)methanediol pinacol ester
  • (2,6-Dimethy|pyridin -3- y|)methanedio| pinaco| ester
CAS:
693774-10-6
MF:
C13H20BNO2
MW:
233.11
Mol File:
693774-10-6.mol
More
Less

3-Hydroxy-2,3-diMethylbutan-2-yl hydrogen (2,6-diMethylpyridin-3-yl)boronate Chemical Properties

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
Light brown to brown Liquid
More
Less

Safety Information

HS Code 
2934999090
More
Less

3-Hydroxy-2,3-diMethylbutan-2-yl hydrogen (2,6-diMethylpyridin-3-yl)boronate Usage And Synthesis

Synthesis

61676-62-8

693774-10-6

Example 2A Synthesis of 2,6-dimethyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine: 3-bromo-2,6-dimethylpyridine (5.10 g, 27.4 mmol) was dissolved in anhydrous ethyl ether (160 mL) under nitrogen protection and cooled to -78°C. Dropwise n-butyllithium (4.1 mL, 10 M hexane solution) was added and stirred at -78 °C for 45 min. Subsequently, an ether solution (20 mL) of 2-isopropoxy-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (10.2 g, 54.8 mmol) was added slowly and dropwise at the same temperature and stirring was continued for 3 hours at -78 °C. Upon completion of the reaction, the reaction was quenched with isopropanol (10 mL) and slowly warmed to room temperature. Saturated aqueous sodium chloride solution (150 mL) was added, and the aqueous phase was separated and extracted with dichloromethane (100 mL x 6) several times. The organic phases were combined, dried and concentrated to give 2,6-dimethylpyridine-3-boronic acid pinacol ester as a light brown oil (6.29 g, 98.4% yield). The product was confirmed by 1H NMR (300 MHz, CDCl3): δ 7.92 (d, J = 7.46 Hz, 1H), 6.96 (d, J = 7.80 Hz, 1H), 2.73 (s, 3H), 2.53 (s, 3H), 1.34 (s, 12H). Mass spectral analysis showed (M + H)+ = 234.

References

[1] Patent: US2007/66588, 2007, A1. Location in patent: Page/Page column 29-30

3-Hydroxy-2,3-diMethylbutan-2-yl hydrogen (2,6-diMethylpyridin-3-yl)boronateSupplier

Beijing Green Guardee Technology CO,.LTD
Tel
010-69706062-8011 15045616674
Email
zhangr@greenguardee.com
Tetranov Biopharm
Tel
13526569071
Email
sales@leadmedpharm.com
T&W GROUP
Tel
021-61551611 13296011611
Email
contact@trustwe.com
SynAsst Chemical.
Tel
021-60343070
Hebei Summedchem Co.,Ltd
Tel
0319-5801333-8008 15630992918
Email
sales@summedchem.com