3-(Morpholino)phenylboronic acid

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3-(Morpholino)phenylboronic acid Basic information
Product Name:3-(Morpholino)phenylboronic acid
Synonyms:[3-(4-Morpholinyl)phenyl]boronic acid;Boronic acid, B-[3-(4-morpholinyl)phenyl]-;[3-(Morpholin-4-yl)phenyl]boronic acid;3-Morpholinophenylboronic acid 97%;3-(Morpholino)phenylboronic acid
CAS:863377-22-4
MF:C10H14BNO3
MW:207.03
EINECS:
Product Categories:Boronate Ester;Boronic Acid;Potassium Trifluoroborate
Mol File:863377-22-4.mol
3-(Morpholino)phenylboronic acid Structure
3-(Morpholino)phenylboronic acid Chemical Properties
Boiling point 439.4±55.0 °C(Predicted)
density 1.24
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka8.74±0.10(Predicted)
AppearanceLight brown to brown Solid
Safety Information
HS Code 2934999090
MSDS Information
3-(Morpholino)phenylboronic acid Usage And Synthesis
Synthesis
Triisopropyl borate

5419-55-6

4-(3-BROMOPHENYL)MORPHOLINE

197846-82-5

3-(MORPHOLINO)PHENYLBORONIC ACID

863377-22-4

Slowly add n-BuLi (98.1 mL, 0.102 mol, 1.6 M hexane solution) dropwise to a stirred solution of 4-(3-bromophenyl)morpholine (16.5 g, 0.068 mol) in anhydrous THF (300 mL) at -70°C to -78°C. Maintaining this temperature, the reaction mixture was continued to be stirred for 2 hours. Subsequently, triisopropyl borate (30.5 mL, 0.150 mol) was slowly added dropwise to the reaction mixture while maintaining the same temperature. The dry ice-acetone bath was removed and the reaction mixture was allowed to gradually warm up to room temperature and stirred continuously at room temperature overnight. Upon completion of the reaction, the mixture was poured into saturated aqueous ammonium chloride solution, diluted with an appropriate amount of water and subsequently extracted with ethyl acetate. The organic phases were combined, dried with anhydrous MgSO4, concentrated under reduced pressure, and the temperature was controlled below 40°C to remove the solvent. The resulting residue was ground with a solvent mixture of hexane and ether to give 3-morpholin-4-ylphenylboronic acid (12 g, 85% yield) as a off-white solid. Mass spectrum (ES+): m/z 208 [M+H]+. 1H NMR (d6-DMSO) δ: 3.05 (4H, m), 3.72 (4H, m), 6.95 (1H, d), 7.18 (1H, t), 7.21 (1H, d), 7.38 (1H, br s), 7.94 (2H, s).

References[1] Patent: WO2011/144577, 2011, A1. Location in patent: Page/Page column 26
[2] Patent: WO2011/144578, 2011, A1. Location in patent: Page/Page column 28; 29
3-(Morpholino)phenylboronic acid Preparation Products And Raw materials
Raw materialsTriisopropyl borate-->4-(3-Bromophenyl)morpholine-->Water-->Ammonium chloride-->n-Butyllithium-->Tetrahydrofuran-->Hexane
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