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2-Iodo-4-nitroanisole

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2-Iodo-4-nitroanisole Basic information
Product Name:2-Iodo-4-nitroanisole
Synonyms:2-IODO-4-NITROANISOLE;2-Iodo-4-ntiroanisole;1-Iodo-2-Methoxy-5-nitrobenzene;2-Iodo-1-methoxy-4-nitrobenzene, 2-Iodo-4-nitrophenyl methyl ether;3-Iodo-4-Methoxynitrobenzene[2-Iodo-4-nitroanisole];2-Iodo-4-nitroanisol;Benzene, 2-iodo-1-methoxy-4-nitro-;2-IODO-1-METHOXY-4-NITROBENZENE
CAS:5399-03-1
MF:C7H6INO3
MW:279.03
EINECS:611-079-1
Product Categories:Aromatic Ethers;Anisoles, Alkyloxy Compounds & Phenylacetates;Iodine Compounds;Nitro Compounds
Mol File:5399-03-1.mol
2-Iodo-4-nitroanisole Structure
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
AppearanceLight brown to brown Solid
InChIInChI=1S/C7H6INO3/c1-12-7-3-2-5(9(10)11)4-6(7)8/h2-4H,1H3
InChIKeyKBQBNJHOTNIGDD-UHFFFAOYSA-N
SMILESC1(OC)=CC=C([N+]([O-])=O)C=C1I
CAS DataBase Reference5399-03-1(CAS DataBase Reference)
Safety Information
HS Code 2909309090
MSDS Information
2-Iodo-4-nitroanisole Usage And Synthesis
Uses2-Iodo-4-nitroanisole is commonly used in organic synthesis, especially as a synthetic intermediate in the fields of medicine and chemical research.
Synthesis
2-Amino-4-nitro anisidine

99-59-2

2-Iodo-4-nitroanisole

5399-03-1

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
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