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2-Nitrochlorobenzene: Difference between revisions

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| Section1 = {{Chembox Identifiers
| Section1 = {{Chembox Identifiers
| ChemSpiderID = 13853953
| ChemSpiderID = 13853953
| SMILES = C1=CC=C(C(=C1)[N+](=O)[O-])Cl
| smiles = C1=CC=C(C(=C1)[N+](=O)[O-])Cl
| 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
| InChIKey = BFCFYVKQTRLZHA-UHFFFAOYAA
| InChIKey = BFCFYVKQTRLZHA-UHFFFAOYAA

Revision as of 15:20, 30 October 2013

2-Nitrochlorobenzene
Names
IUPAC name
1-Chloro-2-nitrobenzene
Identifiers
ChemSpider
ECHA InfoCard 100.001.686 Edit this at Wikidata
  • InChI=1S/C6H4ClNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H
    Key: BFCFYVKQTRLZHA-UHFFFAOYSA-N
  • InChI=1/C6H4ClNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H
    Key: BFCFYVKQTRLZHA-UHFFFAOYAA
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
Toxic, Irritant
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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

  1. ^ a b Gerald Booth "Nitro Compounds, Aromatic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH: Weinheim, 2005. doi:10.1002/14356007.a17_411