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2-CHLORO-5-FLUORO-4-IODOPYRIDINE

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2-CHLORO-5-FLUORO-4-IODOPYRIDINE Basic information

Product Name:
2-CHLORO-5-FLUORO-4-IODOPYRIDINE
Synonyms:
  • 2-Chloro-5-fluoro-4-iodopyridine 98%
  • 2-Chloro-5-Fluoro-4-Iodopyridine98%
  • Pyridine, 2-chloro-5-fluoro-4-iodo-
  • Methyl 7-bromopicolinate
  • 2-CHLORO-5-FLUORO-4-IODOPYRIDINE ISO 9001:2015 REACH
  • 2-CHLORO-5-FLUORO-4-IODOPYRIDINE
CAS:
884494-49-9
MF:
C5H2ClFIN
MW:
257.43
Product Categories:
  • Fluorine series
Mol File:
884494-49-9.mol
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2-CHLORO-5-FLUORO-4-IODOPYRIDINE Chemical Properties

Boiling point:
242℃
Density 
2.129
Flash point:
100℃
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka
-2.37±0.10(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C5H2ClFIN/c6-5-1-4(8)3(7)2-9-5/h1-2H
InChIKey
CRLPRXQOSARJCF-UHFFFAOYSA-N
SMILES
C1(Cl)=NC=C(F)C(I)=C1
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
HS Code 
2933399990
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2-CHLORO-5-FLUORO-4-IODOPYRIDINE Usage And Synthesis

Synthesis

31301-51-6

884494-49-9

The general procedure for the synthesis of 2-chloro-5-fluoro-4-iodopyridine using 2-chloro-5-fluoropyridine as starting material was as follows: 2-chloro-5-fluoropyridine (10.0 g, 76.0 mmol, 1.0 eq.) was dissolved in anhydrous tetrahydrofuran (THF, 100 mL) under nitrogen protection and cooled to -78 °C. Lithium diisopropylammonium (LDA, 58 mL, 116 mmol, 2 M in THF) was added slowly and the reaction mixture was kept stirred at -78 °C for 3 hours. Subsequently, a solution of iodine (I2, 23.2 g, 91.0 mmol) in THF (100 mL) was slowly added at the same temperature. The reaction mixture continued to be stirred at -78 °C for 1 h. The reaction was then quenched with water (200 mL). The reaction mixture was slowly warmed to room temperature and extracted with ethyl acetate (EtOAc, 100 mL x 2). The organic layers were combined, washed with brine (50 mL × 2), dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography with the eluent being petroleum ether (PE) to ethyl acetate/petroleum ether (1/20, v/v) to afford 2-chloro-5-fluoro-4-iodopyridine (11.8 g, 60% yield) as a white solid.1H NMR (400 MHz, CDCl3): δ 8.13 (s, 1H), 7.76 (d, 1H).

References

[1] Patent: WO2017/1936, 2017, A2. Location in patent: Paragraph 00200
[2] Patent: US2017/29404, 2017, A1. Location in patent: Paragraph 0251-0253
[3] Patent: US2014/309225, 2014, A1. Location in patent: Paragraph 0830
[4] Patent: WO2018/49089, 2018, A1. Location in patent: Page/Page column 168
[5] Patent: EP2589592, 2018, B1. Location in patent: Paragraph 0995; 0996

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