Oxidative preparation of aldehydes and ketones WWU Chemistry

Oxidative preparation of aldehydes and ketones WWU -- Chemistry

REMEMBER: • Go back to Special Topics Box at the beginning of Chapter 14. • Conversion of an alcohol to an aldehyde or ketone represents an oxidation (removal of H atoms). • Conversion of an aldehyde to a carboxylic acid is also an oxidation (addition of an O atom). • Oxidation can involve the addition of oxygen atoms or it can involve the removal of hydrogen atoms (dehydrogenation). WWU -- Chemistry

Oxidations NOTE: A dehydrogenation is also a form of oxidation! WWU -- Chemistry

Oxidation of Primary Alcohols The aldehyde can be oxidized in a second step [O] represent an oxidation WWU -- Chemistry

Oxidation of Secondary Alcohols WWU -- Chemistry

Oxidation of Tertiary Alcohols WWU -- Chemistry

Oxidation of Primary Alcohols with KMn. O 4 You can’t pull the aldehyde out of this reaction, so the only product is the carboxylic acid. WWU -- Chemistry

Specifically. . . WWU -- Chemistry

• The aldehyde is formed as an intermediate, but it is unstable under the reaction conditions and cannot be isolated. • There is a color change that accompanies the reaction -- the purple solution (KMn. O 4) changes to a brown mud (Mn. O 2) WWU -- Chemistry

Primary alcohols are oxidized by atmospheric oxygen to aldehydes and carboxylic acids. This reaction is very slow. It is catalyzed by enzymes (Acetobacter) This is how wine turns to vinegar!!! WWU -- Chemistry

Oxidation of Primary Alcohols to Aldehydes • Requires less vigorous oxidation conditions. • We can try to remove the aldehyde from the reaction medium as quickly as it is formed – Generally, the aldehyde has a lower boiling point than either the corresponding alcohol or carboxylic acid • We can also try to find a milder oxidizing agent. WWU -- Chemistry

Dehydrogenation over Copper • This reaction is generally done by passing the vapors of the alcohol through a tube furnace in a stream of inert carrier gas. • This is not a practical laboratory method -- it is better suited to industrial processes. • The reaction stops at the aldehyde stage -- no more removal of hydrogen can take place. WWU -- Chemistry

Oxidation of Primary Alcohols with K 2 Cr 2 O 7 • This reaction can also be done using Cr. O 3 (chromic oxide) in sulfuric acid. • The aldehyde is distilled away from the reaction vessel as quickly as it is formed. If the aldehyde is not removed, it will suffer a second oxidation, and the product will be the carboxylic acid. WWU -- Chemistry

• The acidic conditions keep the chromium in the Cr 2 O 72 - state. • Potassium dichromate is not as powerful an oxidizing agent as is potassium permanganate • Sodium dichromate can be substituted for potassium dichromate -- it makes no difference. • There is a color change during the reaction. The orange color of the dichromate changes to the green of Cr 3+ ion. • This is not the world’s greatest way to prepare an aldehyde! WWU -- Chemistry

Dichromate Oxidation of Ethanol Orange solution Green precipitate WWU -- Chemistry

Secondary alcohols are oxidized to ketones Here, it doesn’t really matter whether you use potassium permanganate, potassium dichromate, nitric acid, sodium hypochlorite (Bleach), or other oxidizing agents. Actually, it does matter, but here we are presenting the simple introduction! WWU -- Chemistry

“Mechanism” of Oxidation WWU -- Chemistry

• The important point about the mechanism is that the loss of the alcohol C-H occurs during the rate-determining step. • What is not well understood is what happens to the chromium after the formation of the ketone. There is some sort of cascading down through a series of oxidation states, but no one is sure exactly how this happens. WWU -- Chemistry

Which would react faster? There is a primary isotope effect -- C-H bond-breaking occurs during the ratedetermining step! WWU -- Chemistry

Tertiary alcohols are not oxidized Under acidic conditions, the only available reaction is dehydration. WWU -- Chemistry

Let’s re-examine methods for oxidizing primary alcohols to aldehydes and secondary alcohols to ketones (and let’s try some modern reactions!) WWU -- Chemistry

Oxidation of Secondary Alcohols Jones Oxidation WWU -- Chemistry

Example WWU -- Chemistry

… but what if you want to make an aldehyde? • The problem is how to stop the oxidation at the aldehyde stage. • We need mild oxidizing conditions -- strong enough to do one 2 -electron oxidation, but not strong enough to do the second 2 -electron oxidation. • We can use the Jones oxidation (potassium dichromate and sulfuric acid) and try to distill the aldehyde out of the reaction vessel before it gets oxidized a second time. WWU -- Chemistry

… but what if you want to make an aldehyde? (Part Two) • Or, we can tinker with the oxidizing agent, to attenuate its properties -- i. e. , we can try to “dial in” the power of the oxidizing agent to just the right level. • Which brings us to. . . WWU -- Chemistry

Oxidation with Chromic Oxide and Pyridine Sarett Oxidation WWU -- Chemistry

The oxidizing reagent is a type of complex between the chromic oxide and the pyridine. WWU -- Chemistry

Preparation of an Aldehyde Note that the reaction does not affect other functional groups. WWU -- Chemistry

Another useful reagent for oxidizing alcohols to aldehydes or ketones -- in good yield (!) -is pyridinium chlorochromate (PCC). WWU -- Chemistry

Oxidation with Pyridinium Chlorochromate “PCC” Oxidation WWU -- Chemistry

The reagent is prepared by dissolving Cr. O 3 in hydrochloric acid and then adding pyridine. The reagent precipitates as a solid, with the formula: WWU -- Chemistry

The reagent is used in nearly stoichiometric ratios to perform oxidations under mild conditions. Because the reagent is mildly acidic, however, it may not be suitable for use with acid-sensitive compounds. WWU -- Chemistry

Example WWU -- Chemistry

Example #2 Getting better! WWU -- Chemistry

Example #3 WOW!!! WWU -- Chemistry

Notice how the other functional groups survive without being changed. WWU -- Chemistry

CHANGE OF GEARS: • Aldehydes can be oxidized to carboxylic acids. • This oxidation can take place under very mild oxidizing conditions. • Aldehydes can be oxidized with such weak oxidizing agents as metal cations, especially: Ag+ Cu 2+ WWU -- Chemistry

The Tollens Test silver mirror This test is specific for aldehydes -- ketones will not react with silver ion. WWU -- Chemistry

The Tollens test is important in carbohydrate chemistry, for proof of structure. WWU -- Chemistry

These monosaccharides cyclize to form hemiacetals WWU -- Chemistry

b-D-(+)-Glucopyranose Notice that this is a hemiacetal WWU -- Chemistry

• The hemiacetal form is in equilibrium with the open-chain free aldehyde form (remember mutarotation? ). • While in the free aldehyde form, glucose can reduce silver ion (give a silver mirror -a positive Tollens test). • Because it can reduce silver ion, glucose is considered a reducing sugar. WWU -- Chemistry

b-D-(-)-Fructofuranose This is a hemiacetal WWU -- Chemistry

• Being a hemiacetal, the cyclic form of fructose is in rapid equilibrium with the open -chain, free ketone form. • Therefore, fructose is also capable of reducing silver ion, and is thus classified a reducing sugar! WWU -- Chemistry

Yeah, but…. • I thought you said that only aldehydes were capable of giving a positive Tollens test, and fructose is a ketone! • There is an exception: a-hydroxyketones also give a positive test! • Fructose is an a-hydroxyketone (go back and check out its structure). WWU -- Chemistry

Maltose: A Disaccharide Position (b) is now an acetal Position (a) is still a hemiacetal Maltose is a reducing sugar WWU -- Chemistry

Sucrose: A Disaccharide Both positions (a) and (b) are now acetals. Neither is in equilibrium with the open-chain free carbonyl form. Sucrose is a non-reducing sugar! WWU -- Chemistry

What about a monosaccharideether (a glycoside)? This is an acetal -- it is not in equilibrium with a free aldehyde form This is a non-reducing sugar WWU -- Chemistry

How do hydride transfer (oxidation-reduction) reactions take place in biological systems? • We can’t use lithium aluminum hydride or pyridinium chlorochromate inside a living cell! • Any reagent has to be water-soluble, capable of being transported across cell membranes, and able to act in concert with an enzyme. WWU -- Chemistry

Nicotinamide Adenine Dinucleotide “NADH” WWU -- Chemistry

• The reactive portion is the hydrogen attached to Carbon #4 of the pyridine ring (see previous slide) • NADH acts as a reducing agent by transfering a hydride from the C-4 position. WWU -- Chemistry

Reduction of Acetaldehyde in Fermentation WWU -- Chemistry

Reduction of Pyruvic Acid in Muscle Tissue WWU -- Chemistry

A biological oxidation would take place as the reverse of the reactions shown. WWU -- Chemistry

WWU -- Chemistry