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887757-48-4

887757-48-4 Structure

887757-48-4 Structure
IdentificationBack Directory
[Name]

4-Difluoromethoxyphenylboronic acid pinacol ester
[CAS]

887757-48-4
[Synonyms]

4-difluoromethoxyphenylboronic
4-Difluoromethoxyphenylboronic acid pinacol ester
2-[4-(difluoromethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-diox...
2-(4-(difluoromethoxy)phenyl)-4,4,5-trimethyl-1,3,2-dioxaborolane
2-(4-(DifluoroMethoxy)phenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
1,3,2-Dioxaborolane, 2-[4-(difluoromethoxy)phenyl]-4,4,5,5-tetramethyl-
[Molecular Formula]

C13H17BF2O3
[MDL Number]

MFCD09878543
[MOL File]

887757-48-4.mol
[Molecular Weight]

270.08
Chemical PropertiesBack Directory
[Boiling point ]

319.3±37.0 °C(Predicted)
[density ]

1.13±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

Light yellow to light brown Solid
[InChI]

InChI=1S/C13H17BF2O3/c1-12(2)13(3,4)19-14(18-12)9-5-7-10(8-6-9)17-11(15)16/h5-8,11H,1-4H3
[InChIKey]

BPFSJXBWEVRJFH-UHFFFAOYSA-N
[SMILES]

O1C(C)(C)C(C)(C)OB1C1=CC=C(OC(F)F)C=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2931900090
Spectrum DetailBack Directory
[Spectrum Detail]

4-Difluoromethoxyphenylboronic acid pinacol ester(887757-48-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-(DIFLUOROMETHOXY)BROMOBENZENE

5905-69-1

Bis(pinacolato)diboron

73183-34-3

4-Difluoromethoxyphenylboronic acid pinacol ester

887757-48-4

A. General procedure for the synthesis of 2-(4-(difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane: Under nitrogen protection, 1-bromo-4-(difluoromethoxy)benzene (1 g, 4.48 mmol), pinacol ester of bis(boronic acid) (1.2 g, 4.71 mmol), potassium acetate (1.3 g, 13.4 mmol), and PdCl2(dppf)-CH2Cl2 adduct (0.18 g, 0.22 mmol) were dissolved in DMF (15 mL) at 90 °C for 1 h. The reaction was stirred. After completion of the reaction, the reaction mixture was diluted with dichloromethane, washed sequentially with water, saturated NaHCO3 solution and brine, and the organic phase was dried with anhydrous MgSO4 and concentrated. The crude product was purified by ISCO fast chromatography (silica gel column, eluent 100:0 to 50:50 hexane/ethyl acetate gradient) to afford the target product 2-(4-(difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.12 g, 3.32 mmol, yield 74.0%) as a brown oil.

[References]

[1] Organic Process Research and Development, 2018, vol. 22, # 4, p. 557 - 561
[2] Patent: WO2010/104830, 2010, A1. Location in patent: Page/Page column 98-99
[3] Patent: US2012/329802, 2012, A1. Location in patent: Page/Page column 33
[4] Patent: US2007/60623, 2007, A1. Location in patent: Page/Page column 49
[5] Patent: WO2009/26276, 2009, A1. Location in patent: Page/Page column 49-50
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