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1357476-67-5

1357476-67-5 Structure

1357476-67-5 Structure
IdentificationBack Directory
[Name]

4-broMo-2-(1,1,1-trifluoro-2-Methylpropan-2-yl)pyridine
[CAS]

1357476-67-5
[Synonyms]

100346
4-broMo-2-(1,1,1-trifluoro-2-Methylpropan-2-yl)
4-Bromo-2-(2,2,2-trifluoro-1,1-dimethylethyl)pyridine
4-broMo-2-(1,1,1-trifluoro-2-Methylpropan-2-yl)pyridine
Pyridine, 4-bromo-2-(2,2,2-trifluoro-1,1-dimethylethyl)-
[Molecular Formula]

C9H9BrF3N
[MDL Number]

MFCD22393679
[MOL File]

1357476-67-5.mol
[Molecular Weight]

268.07
Chemical PropertiesBack Directory
[Boiling point ]

209.3±40.0 °C(Predicted)
[density ]

1.473±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

2.29±0.10(Predicted)
[InChI]

InChI=1S/C9H9BrF3N/c1-8(2,9(11,12)13)7-5-6(10)3-4-14-7/h3-5H,1-2H3
[InChIKey]

XAQNICQGPIHIIH-UHFFFAOYSA-N
[SMILES]

C1(C(C)(C)C(F)(F)F)=NC=CC(Br)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

4-broMo-2-(1,1,1-trifluoro-2-Methylpropan-2-yl)pyridine(1357476-67-5)1HNMR
4-broMo-2-(1,1,1-trifluoro-2-Methylpropan-2-yl)pyridine(1357476-67-5)1HNMR
4-broMo-2-(1,1,1-trifluoro-2-Methylpropan-2-yl)pyridine(1357476-67-5)19FNMR
Hazard InformationBack Directory
[Synthesis]

1.jpg
To a solution of 18-6 (8.7 g, 42.40 mmol, 1 eq) in 1,2-dichloroethane (90 mL) was added Phosphorus(V) oxybromide (18.23 g, 63.60 mmol, 6.47 mL, 1.5 eq). The mixture was stirred at 80°C for 4 hours. TLC (Petroleum ether: Ethyl acetate: Ethanol =4:3:1) showed a part of starting material was remained. Another Phosphorus (V) oxybromide (6.08 g, 21.20 mmol, 2.16 mL, 0.5 eq) was added into the mixture. The reaction mixture was stirred at 80°C for another 3 hours. TLC (Petroleum ether: ethyl acetate: ethanol=4:3:1) showed the starting material was consumed completely. The mixture was combined with another batch (1 g scale) and then poured into ice saturated sodium bicarbonate solution (300 mL) and adjust the pH=7~8. The mixture was extracted with ethyl acetate (100 mLx3). The combined organic layers were washed with brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated in vacuum. The residue was purified by column chromatography (SiO2, Petroleum ether: ethyl acetate=1:0 to 50:11) to give 18-7 (8.5 g, 31.71 mmol, 67.37% yield, 100% purity) as light yellow oil.
[Synthesis]

4-broMo-2-(1,1,1-trifluoro-2-Methylpropan-2-yl)pyridine can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.
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