3-CHLORO-4-IODOPYRIDINE Chemical Properties

Melting point:

104-108 °C

Boiling point:

245℃

Density 

2.052

Flash point:

102℃

storage temp. 

under inert gas (nitrogen or Argon) at 2–8 °C

pka

1.57±0.18(Predicted)

form 

Solid

color 

White to Light yellow to Light orange

λmax

272nm(MeOH)(lit.)

Sensitive 

Light Sensitive

Safety Information

Hazard Codes 

T,Xn

Risk Statements 

22-37/38-41

Safety Statements 

26-36/37/39

WGK Germany 

nwg

HS Code 

2933399990

3-CHLORO-4-IODOPYRIDINE Usage And Synthesis

Uses

3-Chloro-4-iodopyridine, can be used for the preparation of difluoromethylated pyridines. It is also an intermediate for the synthesis of 5-Chloro-4-(trifluoromethyl)-2-pyridinecarboxylic Acid (C421715).

Synthesis

General procedure for the synthesis of 3-chloro-4-iodopyridine using 3-chloropyridine as starting material: lithium diisopropylammonium (LDA, 5.9 mL, 8.88 mmol) was slowly added to a cooled tetrahydrofuran (THF, 30.0 mL) solution of 3-chloropyridine (1.0 g, 8.88 mmol) at -75 °C. The reaction mixture was stirred continuously at -75 °C for 4 hours. Subsequently, iodine (2.2 g, 8.88 mmol) was added and stirring was continued at the same temperature for 1 hour. Upon completion of the reaction, the mixture was quenched with ice water at -70 °C, the organic layer was extracted with ethyl acetate, the organic phases were combined and concentrated to give 0.500 g of the target product 3-chloro-4-iodopyridine. The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6): δ 8.01 (d, J = 5.1 Hz, 1H), 8.14 (d, J = 4.8 Hz, 1H), 8.63 (s, 1H).

References

[1] Angewandte Chemie - International Edition, 2008, vol. 47, # 5, p. 888 - 890
[2] Tetrahedron Letters, 2004, vol. 45, # 42, p. 7873 - 7877
[3] Tetrahedron, 1993, vol. 49, # 1, p. 49 - 64
[4] Patent: US6169086, 2001, A
[5] Patent: WO2008/57209, 2008, A1. Location in patent: Page/Page column 54-55

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