1,3-phenyldiboronic acid, bis(pinacol) ester

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1,3-phenyldiboronic acid, bis(pinacol) ester manufacturers

1,3-phenyldiboronic acid, bis(pinacol) ester Basic information
Product Name:1,3-phenyldiboronic acid, bis(pinacol) ester
Synonyms:1,3-phenyldiboronic acid, bis(pinacol) ester;Benzene-1,3-diboronic acid, pinacol diester;1,3-Phenyldiboronic acid, pinacol ester;1,3-Phenyldiboronic acid;4,4,5,5-Tetramethyl-2-[3-(tetramethyl-1,3,2-dioxa-borolan-2-yl)phenyl]-1,3,2-dioxaborolane;1,3-phenyldiboronic acid, bis(pinacol) ester AldrichCPR;1,3-Benzenediboronic acid bis(pinacol) ester;1,3-Phenylenediboronic Acid Pinacol Ester
CAS:196212-27-8
MF:C18H28B2O4
MW:330.03
EINECS:
Product Categories:
Mol File:196212-27-8.mol
1,3-phenyldiboronic acid, bis(pinacol) ester Structure
1,3-phenyldiboronic acid, bis(pinacol) ester Chemical Properties
Melting point 133.0 to 137.0 °C
Boiling point 430.9±28.0 °C(Predicted)
density 1.03±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility soluble in Methanol
form powder to crystaline
color White to Almost white
InChIInChI=1S/C18H28B2O4/c1-15(2)16(3,4)22-19(21-15)13-10-9-11-14(12-13)20-23-17(5,6)18(7,8)24-20/h9-12H,1-8H3
InChIKeyLLQQCDJVSYEQQQ-UHFFFAOYSA-N
SMILESC1(B2OC(C)(C)C(C)(C)O2)=CC=CC(B2OC(C)(C)C(C)(C)O2)=C1
Safety Information
WGK Germany WGK 3
HS Code 2931900090
Storage Class11 - Combustible Solids
MSDS Information
1,3-phenyldiboronic acid, bis(pinacol) ester Usage And Synthesis
Synthesis
1,3-Dibromobenzene

108-36-1

Bis(pinacolato)diboron

73183-34-3

1,3-phenyldiboronic acid, bis(pinacol) ester

196212-27-8

1. 1,3-dibromobenzene (2.5 g, 10.6 mmol), bis(pinacolato)diboron (6.0 g, 23.5 mmol), Pd(dppf)2Cl2 (0.9 g, 1.2 mmol), and potassium acetate (7.1 g, 72.1 mmol) were added into a reaction flask under the protection of argon. 2. The reaction mixture was degassed with argon for three times, then heated to 85 °C under argon atmosphere and reacted for 18 h. 3. After completion of reaction, it was cooled to room temperature and filtered. 4. The filtrate was extracted with ethyl acetate and the organic phases were combined. 5. The reaction mixture was then heated to 85 °C under argon atmosphere for 18 h. 3. After completion of the reaction, the reaction mixture was cooled to room temperature and filtered. 4. The filtrate was extracted with ethyl acetate and the organic phases were combined. 5. The organic phases were washed with water and saturated saline in turn. 6. The washed organic phases were dried with anhydrous sodium sulfate, filtered, and concentrated. 7. The resultant residue was purified by column chromatography on silica gel using an eluent of 1:9 ethyl acetate/hexanes mixture. 8. The eluent was a 1:9 solvent mixture of ethyl acetate/hexane. 8. The target fraction was collected and concentrated to remove the solvent. 9. The product was recrystallized from a solvent mixture of dichloromethane/methanol to give pinacol ester of 1,3-bis(phenylene diboron) acid as an off-white solid (3.008 g, 86% yield). 10.

References[1] New Journal of Chemistry, 2018, vol. 42, # 6, p. 4728 - 4734
[2] Patent: US2012/226046, 2012, A1. Location in patent: Page/Page column 18; 19
[3] Organic Letters, 2007, vol. 9, # 4, p. 559 - 562
[4] Angewandte Chemie - International Edition, 2016, vol. 55, # 37, p. 11247 - 11250
[5] Angew. Chem., 2016, vol. 128, # 37, p. 11413 - 11417,5
1,3-phenyldiboronic acid, bis(pinacol) ester Preparation Products And Raw materials
Raw materials1,3-Dibromobenzene-->Bis(pinacolato)diboron-->1,4-Dioxane-->Potassium Acetate
Tag:1,3-phenyldiboronic acid, bis(pinacol) ester(196212-27-8) Related Product Information
1,3-phenyldiboronic acid, bis(pinacol) ester 1,3-Benzenediboronic acid