2,6-Difluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoic acid

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2,6-Difluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoic acid Basic information
Product Name:2,6-Difluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
Synonyms:2,6-Difluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoic acid;2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl);3,5-Difluoro-4-carboxyphenylboronic acid, pinacol ester;Benzoic acid, 2,6-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS:1008119-07-0
MF:C13H15BF2O4
MW:284.06
EINECS:
Product Categories:
Mol File:1008119-07-0.mol
2,6-Difluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoic acid Structure
2,6-Difluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoic acid Chemical Properties
Boiling point 370.3±42.0 °C(Predicted)
density 1.26±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka2.23±0.10(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
2,6-Difluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoic acid Usage And Synthesis
Synthesis
4-Bromo-2,6-difluorobenzoic acid

183065-68-1

Bis(pinacolato)diboron

73183-34-3

2,6-Difluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoic acid

1008119-07-0

Under argon protection, 2,6-difluoro-4-bromobenzoic acid (0.4 g, 1.6 mmol), pinacol ester of bisboronic acid (0.5 g, 2.0 mmol), PdCl2(dppf) (0.12 g, 0.17 mmol), and potassium acetate (0.49 g, 4.9 mmol) were dissolved in dioxane (16.5 mL). The reaction mixture was transferred to a sealed vial and degassed twice by vacuum-N2 displacement cycle. Subsequently, the reaction system was heated to 80 °C and the reaction was stirred at this temperature for 21 hours. Upon completion of the reaction, the mixture was cooled to room temperature and filtered through a short column of silica gel to remove solid impurities. The filtrate was concentrated under reduced pressure and purified by fast column chromatography (ISCO 12 g silica gel column with an elution gradient of 20-100% ethyl acetate/hexane) to afford the target product, 2,6-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid, as a brown oil (0.11 g, 19% yield). Mass Spectrometry (ES-) m/z: 283 ([M-H]-); Liquid Chromatography Retention Time: 1.48 min (Analytical HPLC Method D).

References[1] Patent: US2009/75995, 2009, A1. Location in patent: Page/Page column 67
2,6-Difluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoic acid Preparation Products And Raw materials
Raw materials4-Bromo-2,6-difluorobenzoic acid-->Bis(pinacolato)diboron-->1,4-Dioxane-->Potassium Acetate
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