Friedel-Crafts Reaction

Transcription

1 OpenStax-CNX module: m Friedel-Crafts Reaction Mary McHale This work is produced by OpenStax-CNX and licensed under the Creative Commons Attribution License Lab 4: Friedel-Crafts Reaction: Acetylation of Ferrocene 1.1 Objective This experiment features on electrophilic aromatic substitution reaction. In this reaction an electrophile replaces a hydrogen atom in an aromatic compound forming a new carbon-carbon bond. 1.2 Background Information As noted in earlier experiments, a unifying theme of synthetic organic chemistry is the construction of carboncarbon bonds. Such bond-forming reactions allow the elaboration of simpler precursors into more complicated organic structures. Electrophilic aromatic substitution reactions feature an electrophile replacing a hydrogen atom in an aromatic compound and can form a new carbon-carbon bond if done with an electrophilic carbon species. Such reactions were discovered in 1877 by Charles Friedel and James Crafts and are collectively known as Friedel-Crafts reactions. These reactions may be used to introduce both alkyl ("Friedel-Crafts alkylation") and acyl groups ("Friedel-Crafts acylation"). 1.3 Friedel-Crafts Acylation Reaction: Friedel-Crafts acylation represents a powerful and eective way to introduce new carbon-carbon bonds into aromatic compounds. It has been extensively exploited as a synthetic tool since its discovery. However, the reaction is not without limitations. A strong Lewis acid, often aluminum chloride which is corrosive and gives o HCl upon contact with moist air, is required in greater than stoichiometric amounts leading to the generation of considerable quantities of acidic and aluminum contains waste. Common solvents for Friedel-Crafts acylation reactions include halogenated methanes (e.g., dichloromethane) or carbon disulde, representing environmental and/or human health risks. In this experiment, you will use a more benign catalyst, phosphoric acid, to catalyze the Friedel-Crafts acylation reaction. No organic solvents are used, although one of the reactants, acetic anhydride, is used in excess and thus may serve the role as a solvent in this reaction. Unfortunately, these acylation conditions are not general - it is the relatively high reactivity of ferrocene compared to simpler aromatic substrates that allows the replacement of AlCl 3 with phosphoric acid. Discovery of new Friedel-Crafts-like reaction chemistry applicable to simple benzene derivatives remains an area of ongoing investigation. As the following mechanism indicates, Friedel-Crafts acylation involves the formation of an acylium ion as the active electrophilic species. The reactive acylium ion is generated from an acyl halide or anhydride by treatment with a Lewis acid. Aluminum chloride is commonly used for this purpose. Although AlCl 3 could Version 1.2: Oct 16, :01 pm

2 OpenStax-CNX module: m potentially aect the catalysis of the Friedel-Crafts acylation reaction, the product, a ketone, is suciently basic enough to interact strongly with AlCl 3 such that more than one equivalent of AlCl 3 is required. The AlCl 3 is removed in the aqueous workup step by hydrolysis to HCl and aluminum hydroxide. Figure 1 Figure 2 The Friedel-Crafts acylation reaction 1.4 Some Important Points: Acyl groups - carbonyl attached to an H or an alkyl group.

3 OpenStax-CNX module: m Figure 3 Reaction of an aromatic compound with an acyl halide and a Lewis Acid Figure 4 The electrophile is an acylium ion.

4 OpenStax-CNX module: m Figure 5 The para product generally predominates in the acylation of substituted rings. Figure 6

5 OpenStax-CNX module: m Unlike the Friedel-Crafts alkylation, the acylation reaction does not suer from rearrangement of the electrophile nor is the product susceptible to further reaction. - The Freidel Crafts acylation reaction can be used to synthesize alkyl benzenes indirectly. Figure Aromaticity of Organic Compounds: Although many aromatic compounds are based on the prototypical benzene ring system, many other aromatic compounds are known. In general, aromaticity results from a cyclic, planar, fully-conjugated array of atoms with a total of 4n+2 (n = integer) π electrons. Thus neutral compounds such as pyrrole and furan, as well as charged species such as tropylium, cyclopentadienyl and cyclopropenium ions, all represent aromatic compounds. Figure 8 In this experiment, rather than using a simple benzene derivative as a reactant, you will explore the Friedel-Crafts acylation of a cyclopentadienyl ring contained in an organometallic compound (i.e. a compound containing one or more bonds between carbon and a transition metal). The substrate, ferrocene, contains two cyclopentadienyl rings which form a "sandwich" with the central iron atom. Although the presence of the metal atom confers some unusual properties on ferrocene, the cyclopentadienyl rings undergo many reactions typical of aromatic compounds. In particular, ferrocene eciently undergoes Friedel-Crafts acylation and this is the reaction you will investigate.

6 OpenStax-CNX module: m Figure 9 Friedel-Crafts acylation of ferrocene 2 Pre-Lab 4: Friedel-Crafts Reaction (Total 10 points) Click here 1 for the Pre-Lab Name(Print then sign): Lab Day: Section: TA This assignment must be completed individually and turned in to your TA at the beginning of lab. You will not be allowed to begin the lab until you have completed this assignment. 1. Classify each of the following species as anti-aromatic, aromatic, or nonaromatic. Support your answer. (3 points) Figure Show the mechanism for the following reaction. Be sure to include all intermediates. (5 points) 1

7 OpenStax-CNX module: m Figure Predict the products from the following reactions. (2 points) Figure 12 Figure 13

8 OpenStax-CNX module: m Grading You will be assessed on: Completion of pre lab questions. Write-up in your lab notebook Completion of report questions. TA evaluation of lab procedure. 2.3 Materials Equipment Chemicals Water bath Ferrocene Stir bar Acetic anhydride Round bottom ask (10mL) 85% phosphoric acid Hirsch funnel 3 M aq NaOH Beakers (50, 400 ml) NaHCO 3 TLC plates Hexanes Filter paper Toluene, absolute EtOH Safety Phosphoric acid and acetic anhydride are corrosive and acetic anhydride is also a lachrymator. Avoid contact or undue exposure to vapor. Wear gloves all the time, especially when you are working with corrosive reagents. Keep safety glasses on all the time. Dispose of organic substances in their proper containers. 2.4 Experimental Procedure 1. Place 0.25 g. of ferrocene in a 10 ml round-bottom ask containing a magnetic stir bar. Prepare a hot water bath by heating the water to nearly the boiling point while preparing the following reaction mixture. 2. In a fume hood, add 1.0 ml of acetic anhydride and 0.15 ml of 85% phosphoric acid to the ask. The reaction mixture should heat up and darken in color. Swirl the ask, heating occasionally in a hot water bath if necessary, until all the ferrocene dissolves. 3. Attach a reux condenser then heat the reaction mixture with stirring in the hot water bath prepared in step 1. Heat the mixture for 10 minutes during which time a purple color may develop. 2.5 Workup and purication: 4. Pour the reaction mixture onto 2 or 3 cubes of ice in a 400 ml beaker, then rinse the ask with two 5 ml portions of ice water. (A black residue may remain in the ask.) Stir the orange-brown mixture with a glass rod for a few minutes. Any insoluble black material present will be removed in the following steps. 5. Add 6.0 ml of 3 M aqueous NaOH solution, then carefully add solid sodium bicarbonate in small portions until the remaining acid has been neutralized (about 2-3 grams). Use great care to avoid excessive foaming during bicarbonate addition. This step can be done with magnetic stirring, but make sure to use a stirring plate that is not hot. Stir well and crush any lumps to aord a dark-brown suspension. 6. Allow the mixture to stand for 20 minutes, and then collect the crude product by vacuum ltration. Continue to pull air through the product for a few minutes to dry it. Finish the drying process by pressing the solid product between two sheets of lter paper or paper towels. Save some of this crude product for TLC analysis. 7. Transfer the solid and a stir bar to a 50 ml beaker and add 10 ml of hexanes. Boil for 5 minutes with stirring, and then decant the dark-orange solution into another Erlenmeyer ask leaving behind a black gummy substance. If you boil o all the liquid, try again with another 10 ml of hexane and lower heat.

9 OpenStax-CNX module: m To the hot solution, add a spatula-full of decolorizing carbon (If you use too much, you will reduce your yield of carbon). Heat with swirling, and then perform a hot ltration to remove the decolorizing carbon. 9. Set the ask aside to cool slowly. Red-brown needles of acetylferrocene should begin to form. Once the ask has reached room temperature, cool it in ice. Collect the crystalline product by vacuum ltration and washing with a small quantity of cold hexane, then dry by continuing to pull air through the product for a few minutes. If you add to much cold hexane here, you will lose your product Characterization: 10. Record the yield and melting point range for your recrystallized acetylferrocene. 11. Analyze your crude and recrystallized products by TLC. Separately dissolve very small amounts of pure ferrocene, the crude product, and the recrystallized acetylferrocene in a few drops of toluene. Spot the solutions on silica gel plates and develop with 30:1 toluene/absolute ethanol. Visualization is simple as each compound is brightly colored. Safety Wear safety goggles and gloves all the time Waste Disposal Organic compounds must be disposed in the proper container Approximate Lab Time 2 2 ½ hours 3 Report 4: Friedel- Crafts (Total 30 points) (Click here 2 for the Report Form Note: In preparing this report you are free to use references and consult with others. However, you may not copy from other students' work or misrepresent your own data (see honor code). Name(Print then sign): Lab Day: Section: TA 1. Draw the mechanism for the reaction of ferrocene, acetic anhydride, and phosphoric acid. (6 points) 2. Show your theoretical and percent yield calculations for the reaction. (3 points) 3. The melting point of your re-crystallized acetylferrocene is: - (2 points) 4. Draw the TLC plates and show your R f calculations (4 points) 5. Classify each of the following species as anti-aromatic, aromatic, or nonaromatic. Support your answer. (4 points) 2

10 OpenStax-CNX module: m Figure Ordinarily the barrier to rotation about a carbon-carbon double bond is quite high (40 kcal/mol), but the compound below was observed to have a rotational barrier of only about 20 kcal/mol. Explain this result. (3 points) Figure Propose a mechanism for the following reaction. (8 points)

11 OpenStax-CNX module: m Figure 16