Lecture 16 Aromatic Diazonium Salts - nptel

NPTEL – Chemistry – Principles of Organic Synthesis

Lecture 16 Aromatic Diazonium Salts 7.1.1 The Formation of Diazonium Salts Addition of aqueous solution of NaNO2 to a solution of amine hydrochloride in presence of excess of HCl which is cooled by an ice-bath such that the temperature of the reaction remains below 5 ◦C diazotization of primary aromatic amine occurs.

NH2

N2 Cl NaNO2 o HCl,< 5 C

Mechanism

H

HO NO

-OH2

NO HN N OH

HN NO

H2N NO

NH2

-H

H2O NO

NO+

-H

N N OH

N N H

H

N N OH2

-H2O

If electron withdrawing groups are attached to aromatic nucleus then the aromatic amines are difficult to diazotize because the nucleophilicity of the amino-nitrogen is reduced by the partial withdrawal of the unshared electron pair into the nucleus.

Joint initiative of IITs and IISc – Funded by MHRD

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NH2

O

N

NH2

N

O

O

O

7.1.2 The Reaction of Diazonium Salts 7.1.2.1 Reactions of nucleophiles at nitrogen Nucleophiles react with diazonium ions to give covalent diazo-compounds. For example, phenol via phenoxide ion couples with diazonium salt at pH 9-10 to afford paraazophenols in good yield.

N N Ar

H O

O

tautomerizes HO

N N Ar

N

N Ar

7.1.2.2 SN1 Reaction Diazonium salts decompose on warming into nitrogen and aryl cation which is highly reactive and could be attacked by any nucleophile in its vicinity.

N2

-N2

H2O

OH2

-H

OH

warm

7.1.2.3 One Electron Reductions Diazonium ions could be reduced by single electron transfer to give an aryl radical and nitrogen. Copper(I) is frequently used for this purpose and the aryl radical is highly reactive capable of abstracting a ligand from the transition metal ion or a hydrogen atom from a covalent bond. Joint initiative of IITs and IISc – Funded by MHRD

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N2 Cl

CuCl

. + Cl Cu Cl

Cl

-CuCl

-N2

7.2 Reactions in which Nitrogen Eliminated 7.2.1 Replacement by Hydroxyl Diazonium salt on warming in water gives phenol via SN1 mechanism. The reaction is generally performed in acidic solution to preserve phenol in its unionized form.

N2 Cl

OH

H2O/H warm

7.2.2 Replacement by Halogen 7.2.2.1 Schiemann Reaction Treatment of an aqueous solution of diazonium salt with fluoroboric acid under cold conditions gives diazonium fluoroborate as precipitate, which could be dried and gently heated to afford the flurobenzene by decomposition.

The reaction involves SN1

mechanism.

N

N

Cl Aq. MBF4, cold

N

N

BF4

dry ppt

M = Na, H, NH4 salt precipitates - MCl


heat

F

F B F F BF4

-BF3

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F


Examples: NH2 S

F NaNO2, HCl

CO2Me

HPF6

CO2Me S 47%

A. Kiryanov, A. Seed, P. Sampson, Tetrahedron Lett. 2001, 42, 8797.

OH

OH

NaNO2

OH N F F B OH F. Dolle, L. Dolei, H. Valette, F. Hinnen, F. Vaufrey, H. Guenther, C. Fuseasu, C. Coulon, M. Buttalender, C. Crouzel, J. Med. Chem. 1999, 42, 2251. N

NH2

Me

Me NH2

NaNO2, H

Me

HBF4

Br

F Me Br

H. Hart, J. F. Janssen, J. Org. Chem. 1970, 35, 3637.

7.2.2.2 Sandmeyer Reaction This method provides an effective route for the preparation of aromatic bromides and chlorides. Addition of cold aqueous solution of diazonium chloride to a solution of CuCl in HCl medium gives a sparingly soluble complex which is separated and heated to give aryl chloride or bromide by decomposition. NH2 HONO HX X = Br, Cl, CN

N2 X

CuX


. + X-Cu-X + N2

-N2 -CuX

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X


Examples: N NH2 S

Me

N

NaNO2, HCl CuSO4

Cl S 53%

Me

N. Zou, J.-F. Liu, B. Jiang, J. Combin. Chem. 2003, 5, 754. NH2

HONO

Me

CuCN

CN Me

H. T. Clarke, R. R. Reed, Org. Synth. 1941, 1, 514. F

NH2

F

Br

HNO2, CuBr N

N

HBr

O

O

65% B. Mallesham, B. M. Rajesh, P. R. Reddy, D. Srinivas, S. Trehan, Org. Lett. 2003, 5, 7963.

7.2.3 Replacement by Aromatic Carbon A number of methods lead to arylation of aromatic carbon by diazonium salts.

7.2.3.1 Pschorr Reaction This reaction describes the synthesis of phenanthrene and its derivatives via diazotation followed by intramoecular cyclization using copper powder. G NH2

G HNO2, H Cu(0)

G = CH=CH, CH2-CH2, CO, NH, CH2, others


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Mechanism The reactive intermediate depends on the reaction conditions. Under acidic conditions, the diazonium salt is believed to decompose into aryl cation and nitrogen. The aryl cation is highly reactive and attacked by the aryl ring that leads to cyclization. On the other hand, under neutral and basic conditions, the diazonium salt is reduced by single electron transfer to give aryl radical which proceeds reaction intramolecularly with benzene ring to give the cyclized product. In acid solution: G N2

G

G

-N2

H

H

-HH G

Cu(0) + H In neutral or basic solution: G N2

G

Cu(0) -N2

. + Cu(I)


G .

Cu(I) + H

.

H

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Examples: O O NaNO2, H2SO4 Me2N

Cu-Sn, Na2SO4 NMe2

NH2

Me2N

65%

NMe2

S. G. R. Guinot, J. D. Hepworth, M. Wainwright, J. Chem. Res. Synop. 1997, 183,. O

O Bn

HNO2

N N

Bn

N N

H2N P. Tapolcsanyi, B. U. W. Maes, K. Monsieurs, G. L. F. Lemiere, Z. Riedl, G. Hajos, B. Van den Driessche, R. A. Dommisse, P. Maytyus, Tetrahedron 2003, 59, 5919.

7.2.3.2 Reduction by Copper(I) Ammonium Ion Diazotized anthranilic acid with copper(I) ammonium hydroxide gives diphenic acid in 90% yield. CO2H N2 2

CO2H CO2H Cu(NH3)2OH

The process probably takes place via one-electron reduction of the diazonium ion followed by dimerization of the resulting aryl radicals.

7.3 Reactions in which Nitrogen is Retained The reaction of the terminal nitrogen of a diazonium salt with nucleophile affords a covalent azo-compound.

7.3.1 Reduction to Arylhyrazones The reduction of aromatic diazonium salts can be accomplished with sodium sulfite or SnCl2 or electrolysis to provide arylhydrazines. In case of sodium sulfite based reduction, the diazonium ion with a sulfite anion may give a covalent azo-sulfite that, having a double bond conjugated to an electron-accepting group, may add to a second nucleophilic sulfite ion which on hydrolysis provides the hydrazine.


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N N

O

O S

O N

O

H

O S

N

O O S O

O N S O N SO O 3

O N S O N SO O 3

O

2H

H O N S O N SO O

-2SO3

3

N H

NH2

7.3.2 Coupling Reactions Diazonium ions are weak electrophiles, however, they undergo coupling with activated aromatic nuclei such as aryl amines, phenols and aromatic heterocyclic compounds. For example, N,N-dimethylaniline reacts with diazonium ion almost at the para-position. However, the careful control of the pH of the reaction medium is necessary for the success of the process.

.. Me2N

N N-Ar

-H

H N N

Me2N

Me2N Ar

N N Ar

In case of primary and secondary aromatic amines, the reaction preferentially takes place at the nitrogen atoms of the diazonium ions. For example, aniline adds to the aromatic diazonium salt to give diazoaminobenzene.

.. NH2

N N-Ph

NH N N

-H

Diazoaminobenzene


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7.4 The Synthetic Value of Diazo-Coupling 7.4.1 Dye-stuffs Aromatic azo-compounds are coloured. Several of those compounds synthesized by the diazo-coupling are employed as dye-stuffs. These compounds can be classified into three groups. 

First group of azo-compounds are neutral which are used as azoic combination (or ingrain) dyes. An example is para red which is prepared by coupling of 2-napthol with p-nitrobenzenediazonium salt.

NO2

N N O+

OH N N

NO2 Para red



The second group of azo-compounds posses either a sulfonic acid group or an amino group which are generally adsorbed directly on the fiber from aqueous solution. Examples are orange II (an acidic dye) and Bismarck brown R (a basic dye).


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SO3H

N N O+ N N

OH SO3

-

orange II (acidic dye)

Me

H2N N

Me

N

Me

NH2

+

NH2 2

N2

-2H

N

+

N

H2N NH2



N2

Me

NH2

Me Bismarck brown R

Azo-compounds that contain chelating groups to bind with a metal ions such as Al(III) are used a mordant dyes. An example is alizarin yellow R, which contains phenolic and carboxyl chelating groups.

O

OH

Al

CO2H

O O

N2

OH

Al(III)

CO2H +

N N

N N

NO2 NO2


NO2 alizarin yellow R

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7.4.2 Indicators Azo-compounds that contain both an acidic and a basic group can be utilized as indicators since the colours of the conjugate acid and the conjugate base are different. Examples are methyl orange and methyl red which are prepared by coupling of dimethylaniline with diazotized sulfanilic acid and diazotized anthranilic acid, respectively. HO3S

CO2H N

N

N NMe2

Methyl red

N

Methyl orange

NMe2

7.4.3 Synthesis of Amines Azo-compounds are susceptible to hydrogenolysis to give amines. For example, the coupling of 1-naphthol with benzenediazonium chloride gives azo-compound which could be reduced to 4-amino-1-naphthol in the presence of dithionite. OH

O-

OH Na2S2O4

PhN2 N

+ PhNH2 NH2

N Ph

7.4.4 Synthesis of Quinones The ortho and para diamines and aminophenols readily oxidize to give quinones. Both classes of compounds can be readily prepared by diazo-coupling followed by reduction. Ph N N O-

PhN2

+

O

NH2 OH

Na2S2O4

OH

O

FeCl3/O2 Quinone


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Problems:

A. How would you obtain the following compounds? CO2H

HO3S

N

N

N

N

NMe2

NMe2 O

OH

N

N

O

B. Complete the following reactions. O Me

CuI

1. N2

CHO +

2.

O 3.

Cl

CO2Et

CO2H

Ac2O

NaOAc PhN2

Text Books: R.O.C. Norman and C. M. Coxon, Principles of Organic Synthesis, CRC Press, New York, 2009. B. P. Mundy, M. G. Ellerd, F. G. Favaloro Jr, Name Reactions and Reagents in Organic Synthesis, Wiley Interscience, New Jersey, 2005.


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