2-Iodo-4-nitroanisole Chemical Properties

Melting point:

96-98°C

Boiling point:

343.3±27.0 °C(Predicted)

Density 

1.893±0.06 g/cm3(Predicted)

storage temp. 

Keep in dark place,Sealed in dry,Room Temperature

Appearance

Light brown to brown Solid

InChI

InChI=1S/C7H6INO3/c1-12-7-3-2-5(9(10)11)4-6(7)8/h2-4H,1H3

InChIKey

KBQBNJHOTNIGDD-UHFFFAOYSA-N

SMILES

C1(OC)=CC=C([N+]([O-])=O)C=C1I

CAS DataBase Reference

5399-03-1(CAS DataBase Reference)

Safety Information

HS Code 

2909309090

2-Iodo-4-nitroanisole Usage And Synthesis

Uses

2-Iodo-4-nitroanisole is commonly used in organic synthesis, especially as a synthetic intermediate in the fields of medicine and chemical research.

Synthesis

Step A. Synthesis of 2-iodo-1-methoxy-4-nitrobenzene 2-Methoxy-5-nitroaniline (10.0 g, 0.060 mol) was suspended in water (150 mL) and concentrated sulfuric acid (12 mL, 0.22 mol) was added slowly. The temperature of the reaction mixture was maintained below 5 °C under cooling in an ice-salt bath, and a solution of sodium nitrite (4.8 g, 0.070 mol) in water (40 mL) was added dropwise. Subsequently, potassium iodide (16.8 g, 0.101 mol) was added and the mixture was heated to 90 °C and kept for 1 hour. Upon completion of the reaction, it was cooled to 0 °C and deep red crystals were precipitated, which were filtered, washed with water and dried. Purification by silica gel column chromatography (eluent: ethyl acetate/hexane) afforded the target compound 2-iodo-1-methoxy-4-nitrobenzene (13.6 g, 75% yield). 1H NMR (300 MHz, DMSO-d6): δ 8.57 (s, 1H), 8.28 (d, 1H), 7.19 (d, 1H), 3.98 (s, 3H). LCMS (M + H)+: m/z = 280.1 (C7H7INO3).

References

[1] Canadian Journal of Chemistry, 2005, vol. 83, # 3, p. 213 - 219
[2] Patent: US2009/286778, 2009, A1. Location in patent: Page/Page column 79
[3] Chem. News J. Ind. Sci., 1901, vol. 83, p. 285
[4] Journal of the Chemical Society, 1901, vol. 79, p. 1076,1077
[5] P. Ch. S., p. 238

2-Iodo-4-nitroanisole(5399-03-1)Related Product Information

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