Basic information Safety Supplier Related

2-chloro-6-iodobenzoic acid

Basic information Safety Supplier Related

2-chloro-6-iodobenzoic acid Basic information

Product Name:
2-chloro-6-iodobenzoic acid
Synonyms:
  • 2-chloro-6-iodobenzoic acid
  • Benzoic acid, 2-chloro-6-iodo-
CAS:
13420-63-8
MF:
C7H4ClIO2
MW:
282.46
Mol File:
13420-63-8.mol
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2-chloro-6-iodobenzoic acid Chemical Properties

Melting point:
147-149℃ (heptane ethyl acetate )
Boiling point:
333.6±27.0 °C(Predicted)
Density 
2.077±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
solid
pka
1.63±0.10(Predicted)
Appearance
Yellow to brown Solid
InChI
1S/C7H4ClIO2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H,(H,10,11)
InChIKey
KNWHWEKCHWFXFZ-UHFFFAOYSA-N
SMILES
OC(C1=C(Cl)C=CC=C1I)=O
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Safety Information

RIDADR 
2811
WGK Germany 
3
HazardClass 
6.1
PackingGroup 
HS Code 
2916399090
Storage Class
6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications
Acute Tox. 3 Oral
Eye Irrit. 2
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2-chloro-6-iodobenzoic acid Usage And Synthesis

Uses

The following building block was synthesized via a C-H activation method developed by Yu and coworkers. The method was incorporated using the Yu-Wasa Auxiliary (Aldrich 791806) and I2 as the sole oxidant for ortho-iodination from the corresponding benzoic acid derivative.

reaction suitability

reagent type: ligand
reaction type: C-H Activation

Synthesis

118-91-2

13420-63-8

General procedure: In a flame-dried 100 mL round-bottomed flask, 2-chlorobenzoic acid (16.4 mmol, 1.0 eq.), palladium acetate (0.05 eq.), iodobenzene diacetate (1.5 eq.), and iodine (1.5 eq.) were added and dissolved in anhydrous DMF (40 mL), and the reaction system was kept at atmospheric conditions. After sealing the flask with a rubber septum, the reaction mixture was stirred at 100 °C for 24 hours. Upon completion of the reaction, the mixture was cooled to room temperature, diluted with ethyl acetate and subsequently washed with 0.5 N HCl solution (420 mL). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate and finally concentrated in a rotary evaporator. The crude product was purified by silica gel column chromatography (eluent ratio 3:1 hexane/ethyl acetate) to afford the target product 2-chloro-6-iodobenzoic acid.

References

[1] ACS Catalysis, 2018, vol. 8, # 2, p. 920 - 925
[2] Australian Journal of Chemistry, 2015, vol. 68, # 6, p. 912 - 918
[3] Angewandte Chemie - International Edition, 2008, vol. 47, # 28, p. 5215 - 5219
[4] Synthetic Communications, 2005, vol. 35, # 6, p. 799 - 806

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