Carboxylic Acid Derivatives and Nucleophilic Acyl ... · 3 General Reaction Pattern Nucleophilic...
Transcript of Carboxylic Acid Derivatives and Nucleophilic Acyl ... · 3 General Reaction Pattern Nucleophilic...
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Based on McMurry’s Organic Chemistry, 7th edition
Dr M. Mehrdad University of Guilan, Department of
Chemistry, Rasht, Iran
2شیمی آلی
Chapter 21.
Carboxylic Acid Derivatives:
Nucleophilic Acyl Substitution
Reactions
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Carboxylic Compounds
Acyl group bonded to X, an electronegative atom or leaving group
Includes: X = halide (acid halides), acyloxy (anhydrides), alkoxy (esters), amine (amides), thiolate (thioesters), phosphate (acyl phosphates)
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General Reaction Pattern
Nucleophilic acyl substitution
Why this Chapter?
Carboxylic acids are among the most widespread of molecules.
A study of them and their primary reaction “nucleophilic acyl substitution” is fundamental to understanding organic chemistry
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21.1 Naming Carboxylic Acid
Derivatives Acid Halides, RCOX
Derived from the carboxylic acid name by replacing the
-ic acid ending with -yl
or the -carboxylic acid ending with –carbonyl and
specifying the halide
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21.1 Naming Carboxylic Acid
Derivatives Acid Halides, RCOX
Derived from the carboxylic acid name by replacing the
-ic acid ending with -yl
or the -carboxylic acid ending with –carbonyl and
specifying the halide
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Naming Acid Anhydrides,
RCO2COR'
If symmetrical replace “acid” with “anhydride” based on the related carboxylic acid
From substituted monocarboxylic acids: use bis-ahead of the acid name
Unsymmetrical anhydrides— cite the two acids alphabetically
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Naming Acid Anhydrides,
RCO2COR'
If symmetrical replace “acid” with “anhydride” based on the related carboxylic acid
From substituted monocarboxylic acids: use bis-ahead of the acid name
Unsymmetrical anhydrides— cite the two acids alphabetically
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With unsubstituted NH2 group. replace -oic acid or -icacid with -amide,
or by replacing the -carboxylic acid ending with –carboxamide
If the N is further substituted, identify the substituent groups (preceded by “N”) and then the parent amide
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Naming Amides, RCONH2
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With unsubstituted NH2 group. replace -oic acid or -icacid with -amide,
or by replacing the -carboxylic acid ending with –carboxamide
If the N is further substituted, identify the substituent groups (preceded by “N”) and then the parent amide
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Naming Amides, RCONH2
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Naming Esters, RCO2R’
Name R’ and then, after a space, the carboxylic acid
(RCOOH), with the “-ic acid” ending replaced
by “-ate”
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Naming Esters, RCO2R’
Name R’ and then, after a space, the carboxylic acid
(RCOOH), with the “-ic acid” ending replaced
by “-ate”
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Naming Thioesters, RCOSR’ Name like an ester but:
Methyl acetate
Methyl thioacetate
For IUPAC names
• Replace “-oate” or “-carboyxlate” with “thioate” or “-
carbothioate”
• For common names
• add “thio” before the acid name “-ate”
Ethyl butanoate
Ethyl butanthioate
Methyl
cyclohexanecarboxylate
Methyl
cyclohexanecarbothioate
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Naming Acyl Phosphates
Name Acyl group then add -phosphate:
If an alkyl group is attached to a phosphate
name it after the acyl group
Acetyl adenosyl phosphateBenzoyl phosphate
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Nam
ing
Sum
ma
ry:
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21.2 Nucleophilic Acyl Substitution
A tetrahedral
intermediate is
formed and the
leaving group is
expelled to
generate a new
carbonyl
compound,
leading to
substitution
Carboxylic acid derivatives have
an acyl carbon bonded to a
group Y that can leave
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Nucleophilic Acyl Substitution
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Relative Reactivity of Carboxylic Acid
Derivatives Nucleophiles react
more readily with
unhindered carbonyl
groups
More electrophilic carbonyl groups are
more reactive to addition (acyl halides
are most reactive, amides are least)
The intermediate with the
best leaving group
decomposes fastest
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Substitution in Synthesis
We can readily convert a more reactive acid derivative into a less reactive one
Reactions in the opposite sense are possible but require more complex approaches
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General Reactions of Carboxylic
Acid Derivatives
water carboxylic acid
alcohols esters
ammonia or an amine an amide
hydride source an aldehyde or an alcohol
Grignard reagent a ketone or an alcohol
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21.3 Nucleophilic Acyl Substitution
Reactions of Carboxylic Acids
Must enhance reactivity
Convert OH into a better leaving
group
Specific reagents can produce acid
chlorides, anhydrides, esters, amides
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The Leaving Group ( SN2) A good leaving group reduces the barrier to a reaction
Stable anions that are weak bases are usually excellent
leaving groups and can delocalize charge
OC1-Chapter 11
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Poor Leaving Groups If a group is very basic or very small, it prevents reaction
Alkyl fluorides, alcohols, ethers, and amines do not typically undergo SN2 reactions.
Poor Leaving groups can be made into good leaving groups “Tosyl chloride”
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Leaving Group (SN1)
Critically dependent on leaving group
Reactivity: the larger halides ions are better leaving groups
In acid, OH of an alcohol is protonated and leaving group is H2O, which is still less reactive than halide
p-Toluensulfonate (TosO-) is excellent leaving group
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Conversion of Carboxylic Acids
into Acid Chlorides
Reaction with thionyl chloride, SOCl2
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Mechanism of Thionyl Chloride
Reaction
Nucleophilic acyl substitution pathway
Carboxylic acid is converted into a chlorosulfite
which then reacts with chloride
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Conversion of Carboxylic Acids
into Acid Anhydrides
Acid anhydrides can be derived from two molecules of carboxylic acid by strong heating to remove water
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Conversion of Carboxylic Acids
into Esters
Methods include reaction of a carboxylate anion with a primary alkyl halide
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Fischer Esterification
Heating a carboxylic acid in an alcohol solvent
containing a small amount of strong acid produces an
ester from the alcohol and acid
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Mechanism of the
Fischer Esterification
The reaction is an acid-catalyzed, nucleophilic acyl substitution of a carboxylic acid
When 18O-labeled methanol reacts with benzoic acid, the methyl benzoate produced is 18O-labeled but the water produced is unlabeled
*
*
*
*
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When 18O-labeled methanol reacts with benzoic acid, the methyl benzoate produced is 18O-labeled but the water produced is unlabeled
Mechanism of the Fischer Esterification
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Carboxylic Acids
into Amides
Amides difficult to prepare.
Carboxylic acids more easily react with amines to make salts.
Reaction with DCC makes better leaving group that will be kicked out by an amine.
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Carboxylic Acids into Alcohols
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Carboxylic Acids into Alcohols
•Preferred over LiAlH4 due to relative ease and safety.
•BH3 Selectively reduces Carboxylic acids in presence
of nitros
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21.4 Chemistry of Acid
Halides Acid chlorides are prepared from carboxylic acids by
reaction with SOCl2 Reaction of a carboxylic acid with PBr3 yields the acid
bromide
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Reactions of Acid Halides
Nucleophilic acyl substitution
Halogen replaced by OH, by OR, or by NH2
Reduction yields a primary alcohol
Grignard reagent yields a tertiary alcohol
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Hydrolysis: Conversion of Acid
Halides into Acids
Acid chlorides react with water to yield carboxylic
acids
HCl is generated during the hydrolysis: a base is
added to remove the HCl
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Conversion of Acid Halides to
Esters Esters are produced in the reaction of acid chlorides
with alcohols in the presence of pyridine or NaOH.
This is called Alcoholysis
The reaction is better with less steric bulk
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Aminolysis: Conversion of Acid
Halides into Amides
Amides result from the reaction of acid chlorides with
NH3, primary (RNH2) and secondary amines (R2NH)
The reaction with tertiary amines (R3N) gives an
unstable species that cannot be isolated
HCl is neutralized by the amine or an added base
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Reduction: Conversion of Acid
Chlorides into Alcohols
LiAlH4 reduces acid chlorides to yield aldehydes and
then primary alcohols
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Reaction of Acid Chlorides with
Organometallic Reagents
Grignard reagents react with acid chlorides to yield tertiary alcohols in which two of the substituents are the same
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Formation of Ketones from Acid
Chlorides Reaction of an acid chloride with a lithium diorganocopper
(Gilman) reagent, Li+ R2Cu
Addition produces an acyl diorganocopper intermediate, followed
by loss of RCu and formation of the ketone
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21.5 Chemistry of Acid
Anhydrides
Prepared by nucleophilic acyl substitution of a
carboxylate with an acid chloride
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Reactions of Acid Anhydrides
Similar to acid chlorides in reactivity
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Acetylation
Acetic anhydride forms acetate esters from alcohols and N-substituted acetamides from amines
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Timeline of historical events in the development of aspirin
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21.6 Chemistry of Esters
Many esters are pleasant-smelling liquids: fragrant odors of fruits and flowers
Also present in fats and vegetable oils
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Preparation of Esters
Esters are usually prepared from carboxylic acids
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Reactions of Esters
Less reactive toward nucleophiles than are
acid chlorides or anhydrides
Cyclic esters are called lactones and react
similarly to acyclic esters
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Hydrolysis: Conversion of
Esters into Carboxylic Acids
An ester is hydrolyzed by aqueous base or aqueous acid to yield a carboxylic acid plus an alcohol
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Mechanism of
Ester Hydrolysis
Hydroxide
catalysis via
an addition
intermediate
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Mechanism of
Ester Hydrolysis:
Acid catalysed
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Aminolysis of Esters
Ammonia reacts with esters to form amides
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Reduction: Conversion of Esters
into Alcohols
Reaction with LiAlH4 yields primary alcohols
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Mechanism of Reduction of
Esters
Hydride ion adds to the carbonyl group, followed by
elimination of alkoxide ion to yield an aldehyde
Reduction of the aldehyde gives the primary alcohol
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Reaction of Esters with Grignard
Reagents
React with 2 equivalents of a Grignard reagent to
yield a tertiary alcohol
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21.7 Chemistry of Amides
Amides are abundant in all living organisms…proteins,
nucleic acids, and other pharmaceuticals have amid
functional groups
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Preparation of Amides
Prepared by reaction of an acid chloride with ammonia, monosubstituted amines, or disubstituted amines
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Reactions of Amides
Heating in either aqueous acid or aqueous base produces a carboxylic acid and amine
Acidic hydrolysis by nucleophilic addition of water to the protonated amide, followed by loss of ammonia
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Basic Hydrolysis of Amides
Addition of hydroxide and loss of amide ion
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Reduction: Conversion of
Amides into Amines
Reduced by LiAlH4 to an amine rather than an
alcohol
Converts C=O CH2
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Mechanism of Reduction
Addition of hydride to carbonyl group
Loss of the oxygen as an aluminate anion to give an
iminium ion intermediate which is reduced to the
amine
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Uses of Reduction of Amides
Works with cyclic and acyclic
Good route to cyclic amines
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21.8 Chemistry of Thioesters and Acyl
Phosphates: Biological Carboxylic Acid
Derivatives Nucleophilic carboxyl
substitution in nature
often involves a
thioester or acyl
phosphate
Acetyl CoA’s are most
common thioesters in
nature
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21.9 Polyamides and Polyesters:
Step-Growth Polymers Reactions occur in distinct linear steps, not as chain
reactions
Reaction of a diamine and a diacid chloride gives an ongoing cycle that produces a polyamide
A diol with a diacid leads to a polyester
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Polyamides (Nylons)
Heating a diamine with a diacid produces a polyamide called Nylon®
Nylon 66® is from adipic acid and hexamethylene-diamine at 280°C
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Polyesters
The polyester from dimethyl terephthalate and
ethylene glycol is called Dacron® and Mylar® to make
fibers
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Beckmann rearrangement
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Biodegradable Polymers
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Importance
2003- North America
107 billion pounds of
synthetic plastics
produced from
petroleum
Take >50 years to
degrade
Improper disposal and
failure to recycle
overflowing landfills
دفع نامناسب و ناتوانی در ززباله های سرریبازیافت و دفع
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Applications
Industry
Products, films, paper laminates & sheets, bags and containers
Automobiles
Medical
Sutures, ligament replacements, controlled drug release mechanisms, arterial grafts…
ای کنترل شده، پیوند ههای دارویی مکانیسم رباطی، بخیه ها، جایگزین های...شریانی
Household Disposable razors, utensils, diapers, feminine hygiene products,
containers…
،ظروف لوازم بهداشتی زنانه، پوشک بچه، وسایل آشپزیتیغ های یکبار مصرف ،یکبار مصرف
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Carbon Cycle of Bioplastics
CO2
H2OBiodegradation
Carbohydrates
Plastic
Products
Plants
Fermentation PHA Polymer
Photosynthesis
Recycle
Polyhydroxyalkanoate
Structure of poly-(R)-3-
hydroxybutyrate (P3HB),
a polyhydroxyalkanoate
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21.10 Spectroscopy of
Carboxylic Acid Derivatives
Infrared Spectroscopy
Acid chlorides absorb near 1800 cm1
Acid anhydrides absorb at 1820 cm1 and also at 1760 cm1
Esters absorb at 1735 cm1, higher than aldehydes or ketones
Amides absorb near the low end of the carbonyl region
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Nuclear Magnetic Resonance
Spectroscopy
Hydrogens on the carbon next to a C=O are near 2 in the 1H NMR spectrum.
All acid derivatives absorb in the same range so NMR does not distinguish them from each other
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13C NMR
13C NMR is useful for determining the presence or
absence of a carbonyl group in a molecule of
unknown structure
Carbonyl carbon atoms of the various acid
derivatives absorb from 160 to 180