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Saturday, June 1, 2013

Synthesis of p-nitroacetanilide-Nitration-Lu Le Laboratory







        The aromatic nitration of acetanilide is an exothermic reaction ; the temperature must be carefully controlled by chilling, stirring, and the slow addition of reagents. Acetanilide is first dissolved in the solvent, glacial acetic acid, by warming. Glacial acetic acid is used because it is a polar solvent capable of dissolving acetanilide and the acetate ion is a poor nucleophile so no substitution is possible. After the solution is cooled, sulfuric acid is added; however, even with cooling, the temperature of the solution rises almost 40E. Both the acetanilide solution and the nitrating solution (a mixture of HNO3, and H2SO4) must be chilled to about 10EC before the reaction is begun.



To prevent dinitration of the acetanilide, the nitrating mixture is added in small portions to the acetanilide solution (and not vice versa) so that the concentration of HNO3, is kept at a minimum. After all the HNO3, H2SO4 solution has been added, the reaction mixture is allowed to warm slowly to room temperature. If the reaction mixture has been kept excessively cold during the addition, there will be a relatively large amount of unreacted HNO3, present, which may cause the temperature to rise above room temperature. If this should happen, the mixture must be rechilled.



The work-up procedure consists of removal of the acids and crystallization of the product. Every trace of acid must be removed because hydrogen ions catalyze the hydrolysis of the amide to p-nitroaniline or its protonated cation. Most of the acid is removed by pouring the reaction mixture onto ice and water, then filtering the flocculent yellow precipitate of p-nitroacetanilide. The last traces of acetic acid are removed by neutralization. Because bases also catalyze the hydrolysis of amides, the neutralizing agent used is disodium hydrogen phosphate (Na2HPO4). This reagent reacts with acids to yield NaH2PO4. The result is a buffered solution with a pH near neutral.



The crude product is air-dried before crystallization. If all of the acid was removed, the product will be light yellow. A deep yellow to yellow-orange product is indicative of the presence of p-nitroaniline from hydrolysis. Unfortunately, p-nitroaniline is difficult to remove from p-nitroacetanilide by crystallization.



Mechanism


Preparation of Nitronium Ion:




Nitration




Chemicals



1.      Acetanilide: 1.625g



2.      Disodium hydrogen phosphate: 3.75g

3.      95% ethanol: 15mL

4.      Glacial acetic acid: 2.5mL

5.      15M nitric acid: 0.875mL

6.      18.4M sulfuric acid: 3.75mL



Procedure



1.      Place 1.625 g of acetanilide in a Erlenmeyer flask, add 2.5 mL of glacial acetic acid(CAUTION: strong irritant), and warm the flask on a hot plate in a fume hood until the acetanilide dissolves. 
 






2.      Cool the flask in an ice bath to about 20


3.      Add 2.5 mL of cold, conc. sulfuric acid. The temperature of the mixture will rise to about 60. Chill the solution to about 10in an ice bath. (The solution will become very viscous.)



4.      Mix 0.875 mL of conc. nitric acid and 1.25 mL of conc. sulfuric acid in a test tube, and chill the flask in an ice bath. 



5.      When both solutions are cold, slowly add the HNO3, H2SO4 solution, 1 mL at

a time, to the acetanilide solution. Keep the reaction flask in an ice bath so that the temperature of the reaction mixture is maintained between 10-20. Stir the reaction mixture carefully after each addition. The entire addition requires about 15 minutes.

 

6.      After the addition is completed, allow the reaction flask to stand at room temperature for 30 minutes. Monitor the temperature; if it rises above 25, chill the flask in an ice bath. Should the rechilling be necessary, allow the flask to stand for 30 minutes or more at room temperature after the rechilling.



7.      Pour the reaction mixture into a beaker containing 25 mL of water and 6.25 g of cracked ice. 


8.      Using a large Buchner funnel, filter the heavy lemon-yellow precipitate with vacuum. Press out as much aqueous acid from the filter cake as possible with a spatula or clean cork while suction is being applied. The precipitate is voluminous; use care in transferring it to the Buchner funnel or a substantial amount of product will be lost.




9.      Transfer the filter cake to a clean 250-mL beaker, and add 100 mL of 15% aqueous disodium hydrogen phosphate. Stir the mixture to a paste-like consistency and refilter using vacuum. 




   

10.  Wash the beaker with two 30-mL portions of cold water. Finally, wash the filter cake with an additional 50 mL of cold water. Press the filter cake with a spatula or clean cork to remove as much water as possible, then dry the solid overnight on a watch glass. Determine the yield and melting point.
 

 




Experimental Record

Weight of p-nitroacetanilide(Theory)
2.170g
Weight of p-nitroacetanilide
1.650g
Yield
76.0%
Melting Point of p-nitroacetanilide (theory)
216
Melting Point of p-nitroacetanilide
210~214



12 comments:

  1. hen hao
    very precise and correct...
    this has really helped me in my practical

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  2. This comment has been removed by the author.

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  3. why the main -major- product is the para isome ????

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  4. If I am not mistaken, the acetyl derivative of Aniline is also how manufacturers nitrate aniline,in the protected,or rather deactivated form to control nitration of aniline to successively nitrate to get special explosives? they do this for safety and yield I think. I do know that direct nitration of Aniline by itself can lead to destruction of the aromatic ring, or at least thats what one of my old chemistry books says.

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  5. Y was sulphuic acid added to the solution

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    Replies
    1. Sulphuric acid acts as dehydrating agent... it absorbs the water which is produced during nitration.... also sulphuric acid is stronger than nitric acid..so it protonates the nitric acid thus generating nitronium ion,which is the electrophile req for nitration.

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  6. why p-nitroacetanilide is obtained 80% but O-nitroacetanilide is 20%

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