2-Nitrochlorobenzene: Difference between revisions
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| Section1 = {{Chembox Identifiers |
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| ChemSpiderID = 13853953 |
| ChemSpiderID = 13853953 |
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| smiles = C1=CC=C(C(=C1)[N+](=O)[O-])Cl |
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| InChI = 1/C6H4ClNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H |
| InChI = 1/C6H4ClNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H |
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| InChIKey = BFCFYVKQTRLZHA-UHFFFAOYAA |
| InChIKey = BFCFYVKQTRLZHA-UHFFFAOYAA |
Revision as of 15:20, 30 October 2013
Names | |
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IUPAC name
1-Chloro-2-nitrobenzene
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Identifiers | |
ChemSpider | |
ECHA InfoCard | 100.001.686 |
CompTox Dashboard (EPA)
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Properties | |
ClC6H4NO2 | |
Molar mass | 157.5546 grams/mol |
Appearance | yellow crystals |
Density | 1.368 g/L |
Melting point | 33 °C |
Boiling point | 245.5 °C |
Highly soluble In diethyl ether, benzene, and hot ethanol. Insoluble In H2O | |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Toxic, Irritant |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2-Nitrochlorobenzene is an organic compound with the formula ClC6H4NO2.[1]It is a yellow crystalline solid that is important as a precursor to other compounds due to the two reactive sites present on the molecule.
Synthesis
Nitrochlorobenzene is typically synthesized by nitration of chlorobenzene in the presence of sulfuric acid:
- C6H5Cl + HNO3 → O2NC6H4Cl + H2O
This reaction affords a mixture of isomers. Using an acid ratio of 30/56/14, the product mix is typically 34-36% 2-nitrochlorobenzene and 63-65% 4-nitrochlorobenzene, with only about 1% 3-nitrochlorobenzene.
Reactions
Alkylation and electrophilic aromatic substitution can occur at the chlorinated carbon center, and a diverse array of reactions can be carried out using the nitro group.[1]2-Nitrochlorobenzene can be reduced to 2-chloroaniline with Fe/HCl mixture, the Bechamp reduction.
Applications
2-Nitrochlorobenzene is not valuable in itself but is a precursor to other useful compounds. The compound is particularly useful because both of its reactive sites can be utilized to create further compounds that are mutually ortho. Its derivative 2-chloroaniline is a precursor to 3-3’ dichlorobenzidine, itself a precursor to many dyes and pesticides.
References
- ^ a b Gerald Booth "Nitro Compounds, Aromatic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH: Weinheim, 2005. doi:10.1002/14356007.a17_411