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ChemicalBook--->CAS DataBase List--->1084953-47-8

1084953-47-8

1084953-47-8 Structure

1084953-47-8 Structure
IdentificationBack Directory
[Name]

5-Trifluoromethylpyridine-3-boronic acid pinacol ester
[CAS]

1084953-47-8
[Synonyms]

5-Trifluoromethylpyridine-3-boronic acid picol ester
[5-TRIFLUOROMETHYLPYRIDINE-3-BORONIC ACID PICOL ESTER]
5-Trifluoromethylpyridine-3-boronic acid pinacol ester
5-(Trifluoromethyl)pyridine-3-boronic acid, pinacol ester 98%
3-(tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)pyridine
Pyridine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)-
3-hydroxy-2,3-dimethylbutan-2-yl hydrogen (5-(trifluoromethyl)pyridin-3-yl)boronate
[Molecular Formula]

C12H15BF3NO2
[MDL Number]

MFCD12198142
[MOL File]

1084953-47-8.mol
[Molecular Weight]

273.06
Chemical PropertiesBack Directory
[Boiling point ]

313.6±42.0 °C(Predicted)
[density ]

1.18±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

2.80±0.22(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C12H15BF3NO2/c1-10(2)11(3,4)19-13(18-10)9-5-8(6-17-7-9)12(14,15)16/h5-7H,1-4H3
[InChIKey]

LFZDWNHGQKQVIG-UHFFFAOYSA-N
[SMILES]

C1=NC=C(C(F)(F)F)C=C1B1OC(C)(C)C(C)(C)O1
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P271-P280
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

5-Trifluoromethylpyridine-3-boronic acid pinacol ester(1084953-47-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Bis(pinacolato)diboron

73183-34-3

3-Bromo-5-(trifluoromethyl)pyridine

436799-33-6

5-Trifluoromethylpyridine-3-boronic acid pinacol ester

1084953-47-8

The general procedure for the synthesis of 5-trifluoromethylpyridine-3-boronic acid pinacol ester from pinacol ester of biphenylboronic acid and 3-bromo-5-(trifluoromethyl)pyridine was as follows: 3.50 g (15.50 mmol) of 3-bromo-5-(trifluoromethyl)pyridine, 0.54 g (0.8 mmol) of bis(triphenylphosphine)palladium(II) chloride and 4.55 g (46.5 mmol) of potassium acetate were suspended in 75 mL of dioxane and stirred for 15 minutes. Subsequently, 6.42 g (24.8 mmol) of pinacol ester of bisboronic acid (4,4,5,5,4',4',5',5'-octamethyl-[2,2']bis[[1,3,2]dioxaborolane]) was added and the mixture was heated to 100 °C for 20 hours of reaction. Upon completion of the reaction, the mixture was poured into crushed ice, the pH was adjusted to 9-10 with sodium carbonate solution, and then extracted three times with ethyl acetate. The organic phases were combined, washed with water, dried over magnesium sulfate, filtered and concentrated. The residue was purified by fast column chromatography (dichloromethane/methanol, 1:0 to 9:1) to give 3.48 g (82% yield) of 5-trifluoromethylpyridine-3-boronic acid pinacol ester as a colorless solid. Mass spectrum (MS): 273.1 (M+).

[References]

[1] Patent: US2009/48238, 2009, A1. Location in patent: Page/Page column 20
[2] Patent: WO2013/43521, 2013, A1. Location in patent: Page/Page column 38; 39
[3] Patent: EP2719697, 2014, A1. Location in patent: Paragraph 0210-0212
[4] Patent: EP2891656, 2015, A1. Location in patent: Paragraph 0266
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