ChemicalBook--->CAS DataBase List--->243145-83-7

243145-83-7

243145-83-7 Structure

243145-83-7 Structure
IdentificationBack Directory
[Name]

4-Fluorobenzylboronic acid pinacol ester
[CAS]

243145-83-7
[Synonyms]

243145-83-7
2-(4-Fluorobenzyl)
4-Fluorobenzylboronic acid pinacol este
4-fluorobenzylboronic acid pinacol ester
4-Fluorobenzylboronic acid, pinacol ester 95+%
2-(4-Fluorobenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
4-Fluorobenzylboronic acid pinacol ester ISO 9001:2015 REACH
2-[(4-fluorophenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
1,3,2-dioxaborolane, 2-[(4-fluorophenyl)methyl]-4,4,5,5-tetramethyl-
[Molecular Formula]

C13H20BFO3
[MDL Number]

MFCD10698519
[MOL File]

243145-83-7.mol
[Molecular Weight]

236.09
Chemical PropertiesBack Directory
[Boiling point ]

275 °C
[density ]

1.04
[Fp ]

120 °C
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[form ]

liquid
[color ]

Colourless
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2931900090
Questions And AnswerBack Directory
[Application]

In scientific research, boron esters are primarily used as synthetic intermediates in transition metal-catalyzed cross-coupling reactions to construct structurally complex target compounds. In industrial production, boron esters have found wide applications in pharmaceuticals, pesticides, and materials.
Spectrum DetailBack Directory
[Spectrum Detail]

4-Fluorobenzylboronic acid pinacol ester(243145-83-7)1HNMR
4-Fluorobenzylboronic acid pinacol ester(243145-83-7)19FNMR
Hazard InformationBack Directory
[Synthesis]

4-Fluorobenzyl chloride

352-11-4

Bis(pinacolato)diboron

73183-34-3

4-Fluorobenzylboronic acid pinacol ester

243145-83-7

Example 6: Under argon protection, magnesium shavings (16.8 mg, 0.7 mmol) were added to tetrahydrofuran (1 ml), followed by bis(pinacolato)borate (127.0 mg, 0.5 mmol) and p-fluorobenzyl chloride (162 μl, 1.35 mmol). Fe(acac)3 catalyst (3.5 mg, 0.010 mmol, 2 mol%) was added at 0 °C and the reaction was carried out for 3 hours. Upon completion of the reaction, the reaction was quenched with water and the reaction product was extracted with ethyl acetate. The yield of 4-fluorobenzylboronic acid pinacol ester was calculated to be 93% by gas chromatographic analysis.

[References]

[1] Patent: CN107903281, 2018, A. Location in patent: Paragraph 0028
[2] Green Chemistry, 2012, vol. 14, # 3, p. 661 - 667
[3] Journal of the American Chemical Society, 2014, vol. 136, # 27, p. 9521 - 9523
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