Basic information Safety Supplier Related

4-Bromo-6-fluoroquinoline

Basic information Safety Supplier Related

4-Bromo-6-fluoroquinoline Basic information

Product Name:
4-Bromo-6-fluoroquinoline
Synonyms:
  • 4-Bromo-6-fluoroquinoline
  • Quinoline, 4-bromo-6-fluoro-
CAS:
661463-17-8
MF:
C9H5BrFN
MW:
226.05
Mol File:
661463-17-8.mol
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4-Bromo-6-fluoroquinoline Chemical Properties

Boiling point:
299.7±20.0 °C(Predicted)
Density 
1.647±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
2.71±0.16(Predicted)
Appearance
Colorless to yellow Solid
InChIKey
HIWPTYUKGHNQCU-UHFFFAOYSA-N
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-41
Safety Statements 
26-39
WGK Germany 
3
HS Code 
2933499090
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4-Bromo-6-fluoroquinoline Usage And Synthesis

Synthesis

391-78-6

661463-17-8

General procedure for the synthesis of 4-bromo-6-fluoroquinoline from 4-hydroxy-6-fluoroquinoline: To a solution of 4-hydroxy-6-fluoroquinoline (20 g, 122.58 mmol) in DMF (130 mL) heated to 60 °C was slowly added phosphorus tribromide (13 mL, 1.15 equiv.). The reaction mixture was heated at 45 °C with stirring for 45 min. After the reaction was completed, it was cooled to room temperature and the reaction solution was diluted with water (200 mL). Subsequently, Na2CO3 was slowly added until the pH of the reaction solution reached 10. The precipitated solid product was collected by filtration. The solid was dissolved in ethyl acetate (200 mL) and the solution was concentrated to dryness. The residue was purified by column chromatography (eluent: ethyl acetate) to afford the target product 4-bromo-6-fluoroquinoline as a pale yellow solid (22 g, 79% yield).1H NMR (CDCl3) δ: 8.70 (d, J = 4.7 Hz, 1H); 8.14 (m, 1H); 7.96 (d, J = 4.7 Hz, 1H); 7.81-7.73 (m 2H).

References

[1] Patent: WO2008/152603, 2008, A1. Location in patent: Page/Page column 36
[2] Patent: WO2017/21319, 2017, A1. Location in patent: Page/Page column 32

4-Bromo-6-fluoroquinolineSupplier

Nanjing Chemlin Chemical Co., Ltd
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