Synthesis Of Two Useful Organic Compounds Biology Essay

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Objectives: Synthesize two useful organic compounds;

Assess the purity of aspirin by titration against standardized NaOH;

Standardize NaOH and perform a titration;

Enjoy making a natural product.

THE SALICYLATES, ASPIRIN, AND THE BIRTH OF ORGANIC SYNTHESIS:

Organic compounds were so called originally because they were made by living organisms. Now, it is possible to make millions of organic compounds in the laboratory. What they all have in common is a carbon backbone.

FIGURE 1. Aspirin (acetyl salicylic acid): Its Associated Bells & Whistles.

Acetyl Salicylic acid The carbon an acetyl Group A carboxylic acid A Hydroxyl A methyl

backbone Can you find it on aspirin? Group group

of the salicylates

-CH3

Aspirin is one of a class of remarkable analgesic (pain relieving) drugs called the salicylates: (SEE FIGURE 2)

FIGURE 2: SOME OF THE SALICYLATES

BEFORE YOU COME TO LAB:

1. Identify the ACETYL GOUP, THE CARBOXYLIC ACID GROUP, the HYDROXYL GROUP AND THE METHYL GROUP on aspirin and methyl salicylate.

2. Trace the salicylate carbon skeleton on salicylin.

SALICACEAE, Willow Family

The history of medicine has been enriched by thousands of plant species, but one plant--the willow--has probably been used and prescribed more than any other powdered drug. Willow is the original source of aspirin. Even today, when aspirin substitutes are available, up to 80 million tablets of aspirin are used each day in North America, and up to 50 million pounds each year are swallowed throughout the world. Now aspirin can be easily made [industrially] by reacting phenol and carbon dioxide.

Hippocrates of Cos (460-377 B.C.) noted that chewing leaves of willow (Salix) reduced pain, and he prescribed this remedy for women in labor. Hippocrates certainly did not discover this drug, which was used for centuries earlier in European folk medicine. (We should be cautious in crediting Hippocrates with everything because researchers have suggested that the extensive collection of medical writings found in Alexandria, formerly ascribed to Hippocrates, may have been written by several people, the most influential of whom was Hippocrates.) Subsequent ancient Greek physicians recommended willow for alleviating pain and reducing fever and inflammation. In North America, probably even before the Greeks, the Alabama, Chickasaw, and Montagnai Indians used willow to relieve fevers, aches, and pains, and the beneficial effects were also known to the Hottentots of southern Africa.

Advocates of the Doctrine of Signatures described how willow worked to reduce inflammation of joints because the "weeping" branches were very flexible, like human limbs. As late as 1763, an English clergyman named Edward Stone (also known as Edmund Stone) wrote that willow is useful for lowering fever because both willow and fever thrive in damp regions.

In the 1820s, European chemists, eagerly studying the chemistry of plants, were able to isolate from willow a glycoside, which was named salicin, after the genus. Salicin was also discovered in poplars and aspens (also Salicaceae). In the laboratory, Karl Löwig (1839) treated salicin with acid--as salicin is acted on in the human stomach--to make salicylic acid, and about that time salicylic acid was also discovered occurring naturally in a European species of Spiraea (dropwort). Salicylic acid had major medicinal uses and soon became a panacea. A related compound being used at that time was methyl salicylate, found in an oil from birch bark (Betula lenta) and oil of wintergreen (Gaultheria procumbens), long used to relieve aches. In this century, oil of wintergreen was formerly used in "analgesics" (rubefacients) for athletes. [And still is in SportsBalm]

The problem with salicylic acid was that, for many, it caused nausea and great gastric discomfort. A different compound was synthesized in 1853 by Carl von Gerhardt by putting an acetyl group on salicylic acid, making acetylsalicylic acid, which is a chemical salt (solid). Nonetheless, no one was aware of the more gentle properties of this compound until 1893, when Felix Hoffman, an employee of Friedrich Bayer and Company, found an easier way to make this salt and then tested it on his father, who had arthritis. In 1899, Bayer, which started in 1863 as a dye production company, marketed this medicine as "aspirin"--coming from the words 'acetyl' and Spiraea. The price of aspirin initially was expensive until Bayer learned how to mass produce tablets. Aspirin was thus the first major medicine in the world to be sold in tablet form.

As the ancients already knew, aspirin is a remarkable painkiller, i.e., an analgesic. Research indicates that painkilling results from the depressant action of aspirin on the central nervous tissue, somehow by reducing mild to moderate pain messages from reaching the brain. A very important use of aspirin is as an antipyretic, i.e., to lower body temperature (fever), via the dissipation of heat through effects on the hypothalamus, increasing sweating. The third major use of aspirin is as an anti-inflammatory agent (reduce swelling), as for victims of arthritis and "rheumatism."

American consumers spend $700,000,000 to $800,000,000 per year on painkillers (excluding opiates), especially aspirin and acetaminophen, the very common alternative that is marketed under names such as Tylenol, Datril, and Liquiprin. Both chemicals allay pain, but there are important differences. Aspirin, which is significantly cheaper, has the additional anti-inflammatory effects and therefore is critical for arthritis patients (much cheaper than the competing drugs). However, as arthritis pain intensifies, aspirin dosages must also be made stronger, and high dosages are potentially more dangerous. Maximum aspirin daily dosage should be 60 grains per 24 hours.

Medical studies on the effect of aspirin on breaking up blood clots (an antithrombotic drug) are now fairly conclusive, and many physicians prescribe daily aspirin after heart attacks or even as a preventative program because aspirin inhibits release of prostaglandin and thereby platelet agglutination. There are more effective, but not cheaper, antithrombotic drugs, e.g., sulfinpyrazone.

There are over 500 aspirin deaths in this country every year, from large accidental (child) or mostly suicidal (adult) overdoses or, rarely, from allergic reactions. [In 1989, there were 1.28 million ingestion poisonings, of which 5889 were of aspirin, and ten times more of acetaminophen.] Actually, in the United States, children aspirin deaths have declined from 40 to just 2 within the last 20 years. The dangerous side effect of aspirin is gastrointestinal irritation and stomach bleeding, which contribute to stomach ulcers (caused by bacteria). For treating simple aches and pains, painkilling pills that combine aspirin with acetaminophen do not appear to be any more useful than a single chemical.

Perhaps a piece of judiciary history is needed here. Aspirin was a patented name by Bayer, but this German company had conflicts with France and Great Britain, who fought against Germany in World War I and did not acknowledge that patent. Australia also began its own production when aspirin could not be supplied there. A legal battle ensued when Monsanto in the United States began its own production in 1917, and this eventually reached the U.S. Supreme Court, which ruled that "aspirin" had become so widely advertised and common that Bayer no longer owned the name. Hence, aspirin is now a vernacular name, which is why large companies of other products now aggressively take anyone to court when a popular product name is unlawfully used.

Excerpted from: Gibson, A. C. Economic Botany, UCLA, http://www.botgard.ucla.edu/html/botanytextbooks/economicbotany/Salix/

See also: Insel, Paul, "Analgesic-Antipyretics and Antiinflaamatory Agents" in: Goodman &Gilman's The Pharmacological Basis of Therapeutics, 8th ed.,A. G. Goodman, T.W. Rall, A. S. Nies and P. Taylor, eds. McGraw-Hill, NY, 1993.

In this lab, you will synthesis aspirin and oil of wintergreen from salicylic acid:

Balanced equation for the reaction of salicylic acid and acetic anhydride

To make aspirin, you will react salicylic acid with a source of acetyl groups called acetic anhydride. An acetyl group from acetic anhydride reacts with the hydroxyl group on salicylic acid, making an ester, which you will come to know and love in Organic next year.

In the presence of acid and some heat, this reaction occurs quickly. Aspirin is less soluble in water than salicylic acid, and will precipitate out of solution, making it easy to isolate and purify. It won't be pure enough to use against a headache, however.

BEFORE YOU COME TO LAB:

IDENTIFY THE ESTER GROUP ON ASPIRIN.

Next week you will assess the purity of your aspirin by titration.

To make oil of wintergreen, you will use methanol to make an ester, but this time on the carboxylic acid group of salicylic acid. You will find that many esters smell good, and oil of wintergreen is no exception.

BEFORE YOU COME TO LAB:

Where does the methyl group on methanol end up?

We won't do anything further with oil of wintergreen.

Balanced equation for the reaction of salicylic acid and methanol

BEFORE LAB PREPARATION:

Set up a Table of Reagents in your lab notebook, and in Excel. See page 10.

THE EXPERIMENT:

I. SYNTHESIS OF ASPIRIN FROM SALICYLIC ACID:

FIRST things first:

i. Set up a boiling water bath in a 400 or 600 mL beaker on a hot plate.

ii. Start chilling about 100 mL of ice water in a 250 mL beaker.

B. Get the REACTION going:

i. Weigh out 4.0 grams (+/- 0.0001 g) of salicylic acid. (SalH). What is means is: you need more than 3.9 grams and less than 4.1 grams of salicyclic acid, and DO NOT waste your time trying to get exactly 4.0000 grams of salicylic acid. DO record the exact mass of salicylic acid you use, to the nearest 0.0001 g., in your notebook.

Caution: Salicylic acid is a skin irritant. Don't breathe the dust, clean up the balance area and wash your hands.

ii. Clean up the balance.

iii.The TA or lab instructor will dispense for you, in the hood, 10 mL of acetic anhydride. Swirl the flask to mix the SalH, add 10 drops of 18 M (conc) H2SO4, and heat the flask in your boiling water bath for about 15 minutes. Keep an eye out for bumps.

Caution: Acetic anhydride is an eye irritant. Avoid contact with skin & eyes.

Conc. H2SO4 is strongly corrosive. Keep it off your skin, out of your eyes, and in the glass portion of the Pasteur pipet. Keep the pipet straight up & down. Don't tilt it and let sulfuric acid run into the bulb. If you spill any on yourself, wash up with lots of water.

C. While you WAIT: Set up the Oil of Wintergreen prep (part 2).

D. CRYSTALLIZE out the aspirin you made from the rest of the stuff:

Carefully take the reaction flask out of the boiling water bath and add 20 mL of ice water to it. This will decompose excess acetic anhydride:

Put your flask on ice and stir it occasionally until the acetyl salicylic acid has come out of solution. Aspirin (acetyl salicylic acid) is much less soluble in cold water than salicylic acid, which will stay in the supernatant. Crystallization can be speedy and dramatic, with large white crystals crashing out of solution; it can also be spectacularly slow. In general, fast crystallization, while satisfying to the Type A Personality, results in less pure crystals. If you don't see crystals in 5 minutes or so, consult your instructor for tips. If you don't get crystals at all, but see "oiling out", put the flask back in the boiling water bath, reheat it until it no longer looks oily, and cool it again on ice (don't add more ice water).

E. FILTER the solid aspirin away from the rest of the stuff:

Set up a vacuum filter apparatus (there will be a demo apparatus on the front bench), using a Büchner funnel and side arm flask. Put in a piece of filter paper, start the vacuum, and moisten the filter paper with distilled water to seal it down.

Pour the contents of your reaction vessel onto the filter paper. You'll notice that the 2nd law of Lab Science is in effect, namely that a lot of aspirin is sticking to the glass. Rinse the reaction vessel with 10 mL of ice cold water, swirl it around to get the aspirin, and add that to the filter. Repeat one or two more times to get the rest of the aspirin.

If you see any crystals forming in your side arm flask, pour t he filtrate into your reaction vessel , re-assemble the filter, and re-filter.

Wash the aspirin crystals on the filter paper with about 10 mL of ice cold water.

F. RECRYSTALLIZE the aspirin:

The aspirin sitting on your filter paper is mixed with unreacted salicylic acid, and acetic acid and sulfuric acid that haven't washed away. To clean it up:

Scrape the crystals into a 100 mL beaker. Add ethanol, 1 mL at a time, with VIGOROUS SWIRLING…(3rd Law of Lab Science…STIR IT UP!) until the aspirin dissolves. Don't add any more ethanol than you need to (20 mL should do it) and STIR between ethanol additions.

Start about 50 mL of water warming up on a hot plate.

Warm the ethanol/aspirin solution on a hot plate (NO OPEN FLAME) to about 60oC. Pour in about 50 mL of warm water into the ethanol/aspiring solution, stir it, cover it with a watch glass, and set it in an ice bath to crystallize. Aspirin is much less soluble in water than ethanol, and much less soluble in cold water than hot. Salicylic acid is more soluble than aspirin in water, and will stay in solution. You will lose some aspirin in this step, but what you have left will be purer.

Be sure you describe in your notebook what the color and shape of the aspirin crystals are.

G. RECOVER your aspirin, DRY it, WEIGH it and SAVE it for next week.

i. Vacuum filter your crystals, and wash them with two 10 mL portions of ice cold water.

Scrape your crystals into a clean 100 mL beaker, LABEL THE BEAKER with your name & section, cover it with parafilm with holes punched in it, and place it in the area provided. Next week, you will get the mass of the aspirin, calculate the % yield, and assess the purity of your product by titration against standard NaOH.

II. SYNTHESIS OF OIL OF WINTERGREEN:

A. SYNTHESIZE Oil of Wintergreen:

In a 10 mL Ehrlenmeyer flask, mix 0.10 g of salicylic acid with 10 drops (< 0.5 mL) of anhydrous methanol.

Add 1 drop concentrated (18 M ) H2SO4 and a boiling chip, and heat the mixture gently for about 5 minutes.

B. DETECT the product.

Remove the reaction vessel from the heat, stir the mixture with a clean stirring rod, and carefully smell what you have made.

ALL WASTE FROM THIS EXPERIMENT GOES IN THE JUG LABELLED "ORGANIC WASTE" IN THE HOOD

Equipment for 2 students

ASPIRIN

400 or 600 mL Beaker for boiling water bath

(larger size preferred)

Demos: Vacuum filtration apparatus

1

250 mL beaker for ice water

1

125 mL Ehrlenmeyer

1

Ring stand

1

Hot plate

1

Clamp for Ehrlenmeyer neck

1

Ice bath in grey plastic tub

1

Buchner funnel &collar

+ filter paper to fit

1

250 mL Side arm flask &tubing

1

Wash bottles of water

1

100 mL beaker

2

Watch glass

1

10 mL grad cylinder

1

OIL OF WINTERGREEN

10 mL Ehrlenmeyer flask

1

Boiling chip

1

Pastuer pipet &bulb

1

Reagents needed (for 2 students)

ASPIRIN

Salicylic acid

2 g

Acetic anhydride

(dispense small volume for each

section, keep vial tightly closed)

5 mL

Conc. H2SO4

1 plastic

dropper bottle

Ethanol

1 wash bottle

OIL OF WINTERGREEN

Salicylic acid

0.100 g

Methanol

1 plastic dropper bottle

Conc. H2SO4

1 plastic

dropper bottle

SAMPLE REAGENT TABLE FORMAT:

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