Preview

Preparation of Acetanilide

Good Essays
Open Document
Open Document
433 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Preparation of Acetanilide
Synthesis of Acetanilide Reaction
O NH2 + H3C C O O C CH3 O N C CH3 H + H3C O C OH

Aniline

Acetic anhydride

Acetanilide

Acetic acid

Purpose: Acetanilide is a useful precursor to many pharmaceuticals such as acetaminophen and penicillin. Experimental Procedure. (Estimated time: 1.5 h.) Unless otherwise noted, all manipulations should be done in the chemical fume hood. Place 100 µL of aniline into a tared 10 X 75-mm test tube (standing in a small beaker or Erlenmeyer flask). Now add 0.5-mL of distilled water; with swirling, followed by 3 drops of concentrated hydrochloric acid. Add 10 mg of powdered decolorizing charcoal, or the pelletized form (Norit) to the resulting solution. Fit the test tube with a cork stopper and take it back to your hood. Gravity filter this suspension (25-mm funnel fitted with fluted fast-grade filter paper - see instructor) into a 3.0-mL conical vial containing a magnetic spin vane. Wet the filter paper in advance with distilled water and blot the excess water from the stem of the funnel. Use an additional 0.5 mL of distilled water to rinse the test tube and pass that through the filter paper into your vial. Your aniline hydrochloride solution is ready for reaction. Assemble the apparatus as shown below:

CONICAL VIAL W/ MAGNETIC SPIN VANE AND AIR CONDENSER

Dissolve 150 mg (1.10 mmol) of sodium acetate trihydrate in 0.5 mL of distilled water in a 10 X 17-mm test tube. Cap the tube and set the solution aside for use in the next step. Add, with stirring, 150 µL of acetic anhydride to the solution of aniline hydrochloride, followed quickly by addition (Pasteur pipet) of the previously prepared solution of sodium acetate. Stir to thoroughly mix the reagents (~5 min.). You should see the formation of a white precipitate. Allow the reaction mixture to stand at room temperature for approximately 5 min and then place it in an ice bath for an additional 5-10 min to complete the crystallization process. Collect the acetanilide

You May Also Find These Documents Helpful

  • Good Essays

    Also added was 0.45mL water and 0.165mL acetic anhydride and a magnetic spin vane. An air condenser was attached to the vial and it was heated on an aluminum block, with a temperature maintained at 120C. After the solution dissolved, it was heated an extra 20 minutes to allow the reaction to go to completion then cooled back to room temperature. An ice bath was used to encourage crystal growth. The crystals were removed and centrifuged, then placed on a pre-weighed watch glass to dry and weigh. Percent recovery was found. A small sample was set aside for melting…

    • 860 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    Experiment 1 Procedures

    • 537 Words
    • 3 Pages

    Procedure: To a 125 mL Erlenmeyer flask containing a mixture of 95% ethanol (6 mL) and acetic acid (5 mL), dissolve acetanilide (7.4 mmol) and sodium bromide (1.8 g). Place the reaction flask in an ice bath (at least 5oC) for 5 minutes (keep this reaction in the hood). Add sodium hypochlorite (8.3 mmol) by addition of household bleach; leave the reaction flask in the ice bath 5 min. After removing the flask from the ice bath and placing a watch glass over the opening, allow the reaction mixture to come to room temperature over 15 minutes. Place the reaction flask into the ice bath and quench the unreacted bromine by addition of both 5 mL of sodium thiosulfate solution (1 g/5 mL) and 5 mL sodium hydroxide solution(1 g/5 mL ); collect the product by suction filtration. Recrystalllize the brominated product from a minimum amount of solvent. You will need to select a solvent from water, 50% ethanol or 95% ethanol. To identify the best solvent, use what you have learned in Organic I Chemistry Lab, hint: think about what properties makes a good recrystallization solvent. Test your recrystallization solvent in test tubes using the tip of a spatula of your compound. Remember to use a water bath to heat organic solvents. NEVER heat organic solvents directly on a hot plate-always use a hot water bath! Dry the product and obtain melting point range (one fast and one slow) and an IR spectrum. Be sure to record observations in your laboratory notebook.…

    • 537 Words
    • 3 Pages
    Satisfactory Essays
  • Better Essays

    Panacetin Essay

    • 943 Words
    • 4 Pages

    Add 8.0 mL of dichloromethane to the 0.40 g of Panacretin and shake thoroughly, then place in a centrifuge, at three (3) speed for three (3) minutes. Extract the Sucrose and weigh using a digital scale (must be tared for accuracy). Separate the 8.0 mL of DCM to two (2) test tubes, each containing 4.0 mL of DCM. Add 4.0 mL of NaHCO3 (Sodium bicarbonate) to each of the two (2) test tubes and stir using a stirring rod until two (2) layers are visible, a thin top layer and thick-filmy bottom layer. Extract the bottom layers from the two (2) test tubes to a vial using a glass micropipette and a rubber suction cap/top and seal immediately. Conjoin the two (2) top layers to a 50 mL flask and add 1.0 mL of 6.0 M HCl to the beaker containing the solution and stir until the fizzing subsides. Test the pH of the solution with 6.0 M HCl added using pH paper, which has a color chart to analyze the results. Continue to add 1.0 mL of 6.0 M HCl until the pH of the solution is two (2) or less. Place the solution with the pH of 2 or less into an ice bath/cold water bath to form crystallization of aspirin for approximately five (5) minutes. After the five (5) minutes, establish a funnel system using a Hirsche Funnel attached to a vacuum filtration system located on/in the hood, to extract the Aspirin crystals formed from the ice bath/cold water bath. Weigh the crystals of aspirin using a digital…

    • 943 Words
    • 4 Pages
    Better Essays
  • Satisfactory Essays

    Organic Chem

    • 521 Words
    • 3 Pages

    H H3C C H3C CH3 H H C C H H3C C CH3 H3C H C CH3…

    • 521 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    A TLC chamber was then assembled by using a beaker slightly filled with solvent, 3:6:1 Toluene: EF2O: MeOH. Plates were then spotted along the line at the bottom, using capillary tubes, each with a sample of acetaminophen, acetylsalicylic acid, and caffeine. Then each plate was individually spotted with a different pill sample that was dissolved in the acetone. These plates were then placed in TLC chambers and allowed the solvent to travel up the plate. Once close to the top, the plate was taken out of the chamber and a line was drawn where the solvent stopped.…

    • 473 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Dry, sublimed ferrocene (93 mg) was added to a reaction tube. Later, 0.35 mL of acetic anhydride and 0.1 mL of 85% phosphoric acid were also added. The reaction tube was capped using a septum, and a syringe needle was poked through. This was warmed over a steam bath and stirred for 10 minutes after it began to boil, forming a dark brown color. The tube was then cooled to room temperature, then further cooled in ice. A solution of 0.5mL was added, dropwise w/ mixing. 3M NaOH was added until the pH of the solution was neutral. The product was vacuum filtrated and pressed dry.…

    • 850 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Weigh a reaction tube while it is in a 50-mL beaker. Record the mass of the beaker and the tube. Place 0.809 g isopentyl alcohol in a test tube using a Pasteur pipette. Then, add 2 mL acetic acid and 3 drops concentrated sulfuric acid to the tube. Add a boiling chip, then wrap a wet Kim-wipe around the top of the test tube. Place the tube in a sand bath on a setting of 2-3. Heat to boiling, then reflux solution for 1 hour.…

    • 1240 Words
    • 5 Pages
    Good Essays
  • Better Essays

    The electrophilic aromatic substitution reaction is the attack of a benzene ring on an electrophilic species resulting in the substitution of a proton with a functional group. The electrophilic aromatic substitution reaction nitration is used to nitrate methyl benzoate and acetanilide with a nitronium ion. Crystallization was used to purify the product. The melting point was used to determine its purity and the regiochemistry of the products. The methyl benzoate reaction product, methyl nitrobenzoate, was determined to be meta-substituted and the acetanilide reaction product, nitroacetanilide, was determined to be para-substituted.…

    • 3498 Words
    • 14 Pages
    Better Essays
  • Satisfactory Essays

    Making Ethyl Ethanoate

    • 409 Words
    • 2 Pages

    This experiment would produce an atom economy of 100%, as there is one reactant making one product meaning there are no waste products produced. Although this experiment would be extremely efficient in producing ethyl ethanoate, it is a dangerous experiment to conduct therefore I would not recommend the company to use this method to produce ethyl ethanoate as the risk is too high.…

    • 409 Words
    • 2 Pages
    Satisfactory Essays
  • Satisfactory Essays

    Figure 2: IR spectrum of recovered esterfication; isopentyl acetate. Relevent peak frequencies include formation of 1743.25 of ester formation. No large abundant peak of alcohol frequencies 3400-320…

    • 564 Words
    • 3 Pages
    Satisfactory Essays
  • Satisfactory Essays

    The OH group on the benzene ring in salicyclic acid reacts with acetic anhydride to form an ester functional group. Thus the formation of acetylsalicyclic acid (aspirin) is referred to as an esterification reaction, which requires the presence of H+ (H2SO4 in our case). The technique used to purify the aspirin content is called crystallization, which consists in allowing the reaction to cool, decreasing the solubility of acetylsalicyclic acid and allowing it to crystalize. To purify the product even more a recrystallization procedure will be performed. Since salicyclic acid is considered a phenol, a Ferric Chloride test (shows the presence of phenols by changing color from orange to different concentrations of purple, the darker it is the more concentration of phenol is present.) will be performed at the beginning of the experiment and also after each crystallization in order to demonstrate the presence of phenols in the results and thus the purity of the product. A melting point range will also be performed in order to verify the purity of the product.…

    • 292 Words
    • 2 Pages
    Satisfactory Essays
  • Satisfactory Essays

    religion

    • 1284 Words
    • 6 Pages

    O=O 496 6 2976 C-O 366 1 366 O-H 463 1 463 Total 8557 Total 11046…

    • 1284 Words
    • 6 Pages
    Satisfactory Essays
  • Good Essays

    Aspirin Lab

    • 648 Words
    • 3 Pages

    for the procedure I prepared a boiling bath using a hot plate, and filled a 400ml beaker with tap water. Then I got a 125ml Erlenmeyer flask and put in 2.00 grams of Salicylic acid using a scale. For the third step I added 5ml of Acetic Anhydride using a graduated cylinder. Then I added 5 drops of concentrated Sulfuric acid to the Acetic Anhydride and Salicylic acid in the Erlenmeyer flask using a dropper. I then heated the flask in the boiling bath for exactly 10 minutes. I then removed the flask and allowed it to cool on the counter for 4.5 minutes while adding 2 ml of cold distilled water dropwise. I then stirred to mix the contents. I Then added 40ml of distilled water in the solution and stirred until crystals began to form. My crystals formed in a matter of seconds. I then put the flask in a 400ml beaker of ice water to cool it down from room temperature for exactly 10 minutes to complete the crystallization process. I then collected the product in a filtration process by using filter paper and washing out the flask with distilled…

    • 648 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Student

    • 2040 Words
    • 9 Pages

    Draw a ring around the correct answer. The formula of an ammonia molecule is NH3 N3H NH3 (1 mark)…

    • 2040 Words
    • 9 Pages
    Good Essays
  • Satisfactory Essays

    To find the limiting reagent we need to find the number of moles of acetanilide, and the number of moles of Bromine.…

    • 368 Words
    • 2 Pages
    Satisfactory Essays