4-Chlorophenyl azide: Difference between revisions

4-Chlorophenyl azide
Names
	IUPAC name 1-Azido-4-chlorobenzene
	Other names 4-chlorophenylazide
Identifiers
CAS Number	3296-05-7;
3D model (JSmol)	Interactive image;
ChemSpider	69259 ;
PubChem CID	76803;
CompTox Dashboard (EPA)	DTXSID60186612 ;
	InChI InChI=1S/C6H4ClN3/c7-5-1-3-6(4-2-5)9-10-8/h1-4H Key: HZVGOEUGZJFTNN-UHFFFAOYSA-N ;
	SMILES Clc1ccc(\N=[N+]=[N-])cc1;
Properties
Chemical formula	C6H4ClN3
Molar mass	153.569 g/mol
Appearance	Brown solid
Density	1.2634 g/cm3
Melting point	20oC
Boiling point	96oC
Solubility in water	Insoluble in H2O; Soluble in diethyl ether
Hazards
NFPA 704 (fire diamond)	2 3 0
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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Revision as of 22:19, 11 April 2013

4-Chlorophenyl azide is an organic aryl azide compound with the chemical formula C₆H₄ClN₃. The geometry between the nitrogen atoms in the the azide functional group is approximately linear while the geometry between the nitrogen and the carbon of the benzene is trigonal planar.

Preparation

There are various methods to synthesize aryl azides. One such method would be to set use react aniline with Sodium nitrite (NaNO₂) and hydrazine hydrate in the presence of acetic acid^[1]. This reaction will give moderate to good yield of the desired aryl azide. The best solvent for this reaction is dichloromethane. Dichloromethane methane is most effective because it is only slightly polar whereas highly polar solvents give significantly lower yields in this reaction. The reactants dissolve in a less polar solvent better and the reaction proceeds more fully towards completion. Two equivalents of sodium nitrite should be used with five equivalents of hydrazine hydrate to get a high yield of aryl azide. To form 4-chlorophenyl azide specifically, an aniline with a chloride group in the para position is used. The sodium nitrite reacts with aniline to form a diazonium salt that perfroms nucleophilic substitution with the azide ion formed by another reaction between sodium nitrite and hydrazine hydrate in an acidic medium. Such a reaction takes around 30 minutes to complete and gives around an 80% yield. This is an effective method of synthesis because of the short reaction time, easy work-up and inexpensive reagents.

Another synthesis method that was researched was the Wong Synthesis which makes use of the reagents NaN₃ and Tf₂O.^[2] The study of this synthesis method was very detailed because NaN₃ is known to be explosive so careful attention to the synthesis procedures must be used. Researchers found a variation of the Wong Synthesis, replacing NaN₃ with the reaction between aniline, sodium nitrite, and hydrazine. This reaction was timed to take about 35 minutes for the synthesis of 4-chlorophenyl azide. In this reaction the amine substitued aromatic compound is the compound from which the reaction starts. In addition, researchers found an 80% yield of 4-chlorophenyl azide using this variation of the Wong Synthesis.

Reactions

Azides are used in a variety of useful reactions and syntheses. In many different reactions they act as an intermediate step to convert a substituent group to an amine. The reason why using azides is useful in this process is because one of the products of reaction is nitrogen gas (N₂). When a reaction produces gas there is a thermodynamically favorable push towards the products of the reaction. This relates to 4-chlorophenyl azide because this molecule is an intermediate during the formation of 4-chlorophenyl amine. In many instances lithium aluminum hydride (LAH) is used to reduce the azide functional group. An example of this reaction is the following:

Upon further reactions from the above synthesis, 4-chlorophenyl azide can also lead to the useful transformation of the iminium ion. The iminium ion is important in organic syntheses because it reacts similarly like a carbonyl compound. A partial positive charge builds up on the carbon that is doubly bound to the nitrogen which provides an excellent site for nucleophilic attack. An simple way to make the iminium ion is to react an amine with formaldehyde so water leaves the reaction and favors the iminium creation. An example of this reaction is seen below:

Applications

The use of azides is very important in a variety of different applications in organic and biological chemistry. Azides are used in the research of drug applications, in materials science, and also all throughout biology. A majority of the research that is conducted on azides pertains to the catalyst that is needed to create the azide itself. Previously stated, LAH was used for the conversion of the amine to the azide, but this is not always the most environmentally beneficial way of forming the desired product. Research is conducted in many different biological environments to see if a certain catalyst will be recyclable and/or environmentally friendly.

One specific application of 4-chlorophenyl azide is in Friedel Crafts acylation and alkylation. The azide on 4-chlorophenyl azide acts as an electron withdrawing group since the azide has a partial positive charge that is withdrawing electrons from the ring. This means that the azide substituent acts as a meta director in Friedel Crafts acylation and alkylation. Consequently, the chloride on 4-chlorphenyl azide is a deactivating agent, but it also directs to the ortho/para positions on the aromatic ring. Due to the substituent effects on 4-chlorophenyl azide, acylation and alkylation would yield a major product that is newly substituted in the 3 and 5 positions on the aromatic ring. An example of this reaction is given below:

Structure and Bonding

4-chlorophenyl azide is an aryl azide. This is a benzene ring with an azide group and a chloride ion connected in the para position. The azide group is characterized by three nitrogen atoms connected together by two double bonds and is isoelectric with CO₂. This forms a positive charge on the middle nitrogen and negative charges on the outside nitrogens. This extra charge on the outside is important for the release of nitrogen gas (one of the important applications mentioned above).

References

[1] ttp://www.sciencedirect.com.proxy2.library.illinois.edu/science/article/pii/S0040403912022654?np=y

[2] ttp://www.sciencedirect.com/science/article/pii/S0040403912022654

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 == Structure and Bonding ==
--chlorophenyl azide is an aryl azide[[Azide]]. This is a benzene ring with an azide group and a chloride ion connected in the para position. The azide group is characterized by three nitrogen atoms connected together by two double bonds and is isoelectric with CO<sub>2</sub>. This forms a positive charge on the middle nitrogen and negative charges on the outside nitrogens. This extra charge on the outside is important for the release of nitrogen gas (one of the important applications mentioned above).
+-chlorophenyl azide is an aryl [[azide]]. This is a benzene ring with an azide group and a chloride ion connected in the para position. The azide group is characterized by three nitrogen atoms connected together by two double bonds and is isoelectric with CO<sub>2</sub>. This forms a positive charge on the middle nitrogen and negative charges on the outside nitrogens. This extra charge on the outside is important for the release of nitrogen gas (one of the important applications mentioned above).
 == References ==