3-Bromo-2-fluoropyridine
3-Bromo-2-fluoropyridine Basic information
- Product Name:
- 3-Bromo-2-fluoropyridine
- Synonyms:
-
- 2-fluoro-3-bromopyridine
- broMo-3 fluoro-2 pyridine
- 2--3-pyridyl broMidefluoride
- 2-fluoro -3-pyridyl broMide
- 3-BROMO-2-FLUOROPYRIDINE
- 3-Bromo-3-Fluoropyridine
- 3-Bromo-2-fluoropyridine >
- 3-Bromo-2-fL
- CAS:
- 36178-05-9
- MF:
- C5H3BrFN
- MW:
- 175.99
- EINECS:
- 672-944-7
- Product Categories:
-
- blocks
- Bromides
- FluoroCompounds
- Pyridines
- Pyridine
- Pyridine series
- Fluorine series
- Halides
- Variety of halogenated heterocyclic series
- Fluorin-contained pyridine series
- Mol File:
- 36178-05-9.mol
3-Bromo-2-fluoropyridine Chemical Properties
- Boiling point:
- 76°C
- Density
- 1.729
- refractive index
- 1.5370-1.5410
- Flash point:
- 54℃
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- clear liquid
- pka
- -2.79±0.10(Predicted)
- color
- Colorless to Light yellow
- CAS DataBase Reference
- 36178-05-9(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 22-37/38-41
- Safety Statements
- 26-39
- RIDADR
- 2810
- HazardClass
- 6.1
- HazardClass
- IRRITANT
- PackingGroup
- Ⅲ
- HS Code
- 29333990
3-Bromo-2-fluoropyridine Usage And Synthesis
Chemical Properties
Light yellow liquid
Synthesis
52200-48-3
36178-05-9
GENERAL METHOD: 2,3-Dichloropyridine (1.00 g, 6.76 mmol) was dissolved in DMSO (33.8 mL) at room temperature, followed by the addition of CsF (2.053 g, 13.51 mmol). The reaction mixture was stirred at 110 °C for 20 h in air. Upon completion of the reaction, the reaction mixture was quenched with ice water and extracted with EtOAc. The organic layer was separated, washed sequentially with water and brine, dried over anhydrous Na2SO4 and subsequently concentrated under reduced pressure. Purification of the residue by column chromatography (silica gel as stationary phase and EtOAc in hexane as eluent) afforded 3-chloro-2-fluoropyridine (0.639 g, 4.86 mmol, 71.9% yield) as a colorless oil. Compounds 3B'-8B' were prepared by a method similar to the synthetic procedure described above for 2B'.
References
[1] Tetrahedron Letters, 2015, vol. 56, # 44, p. 6043 - 6046
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