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Transcript of Created by Professor William Tam & Dr. Phillis Chang Ch. 20 - 1 Chapter 20 Amines.
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Created byProfessor William Tam & Dr. Phillis
Chang Ch. 20 - 1
Chapter 20Chapter 20
AminesAmines
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Ch. 20 - 2
About The AuthorsAbout The Authors
These PowerPoint Lecture Slides were created and prepared by Professor William Tam and his wife, Dr. Phillis Chang.
Professor William Tam received his B.Sc. at the University of Hong Kong in 1990 and his Ph.D. at the University of Toronto (Canada) in 1995. He was an NSERC postdoctoral fellow at the Imperial College (UK) and at Harvard University (USA). He joined the Department of Chemistry at the University of Guelph (Ontario, Canada) in 1998 and is currently a Full Professor and Associate Chair in the department. Professor Tam has received several awards in research and teaching, and according to Essential Science Indicators, he is currently ranked as the Top 1% most cited Chemists worldwide. He has published four books and over 80 scientific papers in top international journals such as J. Am. Chem. Soc., Angew. Chem., Org. Lett., and J. Org. Chem.
Dr. Phillis Chang received her B.Sc. at New York University (USA) in 1994, her M.Sc. and Ph.D. in 1997 and 2001 at the University of Guelph (Canada). She lives in Guelph with her husband, William, and their son, Matthew.
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Ch. 20 - 3
1. Nomenclature
NH2NH2
Butylamine Cyclohexylamine
1o Amines
Butylethylamine
N
HDiethylamine
N
H
2o Amines
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Ch. 20 - 4
3o Amines
Triethylamine
N
Butylethylmethylamine
N
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Ch. 20 - 5
1A.1A. ArylaminesArylamines
Aniline N,N-Dimethylaniline
NH2 N
NH2
CH3
p-Toluidine(4-Methylbenzeneamine)
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Ch. 20 - 6
1B.1B. Heterocyclic AminesHeterocyclic Amines
Aziridine Pyrrole
NN
N
N N
HH
H
Pridine
Indole Quinoline
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Ch. 20 - 7
2. Physical Properties and Structure of Amines
2A.2A. Physical PropertiesPhysical Properties
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Ch. 20 - 8
2B.2B. Structure of AminesStructure of Amines
NR1
R2
R3
N: sp3 hybridized
Trigonal pyramidal
Bond angles close to 109.5o
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Ch. 20 - 9
3o Amines with three different groups
N
R1
R2
R3
N
R1
R2
R3
● The two enantiomeric forms interconvert rapidly Impossible to resolve
enantiomers● Pyramidal or nitrogen inversion
Barrier ~ 25 kJ/mol Enough to occur rapidly at room
temperature
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Ch. 20 - 10
Ammonium salts with four different groups
N
R1
R2
R3
N
R1
R2
R3
R4 R4
X X
enantiomerscan be resolved
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Ch. 20 - 11
3. Basicity of Amines:Amine Salts
RNH3+ + H2O RNH2 + H3O
+
Ka =[RNH2][H3O
+]
[RNH3+]
pKa = log Ka
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Ch. 20 - 12
The aminium ion of a more basic amine will have a larger pKa than the aminium ion of a less basic amine
H
NH H
H
H
NCH3 H
H
H
NCH3CH2 H
H
Aminiumion pKa
9.26 10.64 10.75
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Ch. 20 - 13
NR H
H
+ H OH
H
NR H
H
OH2+> >
By releasing electrons, R— stabilizes the alkylaminium ion through dispersal of charge
>
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Ch. 20 - 14
(CH3)3N > (CH3)2NH > CH3NH2 > NH3
3o 2o 1o
Gas phase
(CH3)2NH > CH3NH2 > (CH3)3N > NH3
2o 1o 3o
Aqueous solution
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Ch. 20 - 15
3A.3A. Basicity of ArylaminesBasicity of Arylamines
H
NH H
Aminiumion pKa
10.64 4.58 5.08
H
NH H
H
NH H
CH3
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Ch. 20 - 16
NH2 NH2 NH2
NH2NH2
●Five resonance structures
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Ch. 20 - 17
NH2
+ H2O
NH3
+ OH
Aniliniumion
NH3 NH3
●Only two resonance structures
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Ch. 20 - 18
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Ch. 20 - 19
3B.3B. Basicity of Heterocyclic AminesBasicity of Heterocyclic Amines
N
N
N NN
H HH
Order ofBasicity: >> >
pKa of theconjugate acid: 11.2 7 5.2 0.4
(c.f. Et3N, pKa of the conjugate acid = 9.7)
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Ch. 20 - 20
N N NHH
H
H
H H
•
(lost of aromaticity)
+ H+
N
N
N
N
N
N
H H
H
H
HN
N
H
H
+ H+
(still aromatic)Imidazole(a very commonbase in organic
synthesis)
•
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Ch. 20 - 21
3C.3C. Amines versus AmidesAmines versus Amides
O
R NH2
: :
:
O
R NH2
: :
:
:
O
R NH2
: :
:Amide
N-Protonated AmideO
R NH3
: : O
R NH3
: ::
Amides are far less basic than amines (even less basic than arylamines). The pKa of the conjugate acid of a typical amide is about zero
Larger resonance stabilizati
on
Smaller resonance stabilizati
on
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Ch. 20 - 22
O
R NH2
:
O
R NH3
+ OH+ H2O
NH2
:
NH3 + OH+ H2OR R
<
>
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Ch. 20 - 23
3D.3D.Aminium Salts and QuaternaryAminium Salts and QuaternaryAmmonium SaltsAmmonium Salts
R2
NR1 R3 + H Cl
R2
NR1 R3 + R4 Br
H2O
R2
NR1 R3
H(aminium salt)
Cl
R2
NR1 R3
R4
(quaternaryammonium salt)
Br
However, R4N⊕ ⊖OH are
strong bases (as strong as NaOH)
Cannot actas bases
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Ch. 20 - 24
3E.3E. Solubility of Amines in AqueousSolubility of Amines in AqueousAcidsAcids
R2
NR1 R3 + H X
R2
NR1 R3
H(water soluable)
X
O
R NH2
water-insoluableHX
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Ch. 20 - 25
3F.3F. Amines as Resolving AgentsAmines as Resolving Agents Enantiomerically pure amines are
often used to resolve racemic forms of acidic compounds by the formation of diastereomeric salts
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Ch. 20 - 26
OH
O
HO HHO
O
OHH
(R) (S)
H2N
HH3C
(R)-Amine (optically pure)
+
Racemic (R,S)-acid This is the resolving agent
O
O
HO H
(R)
H3N
HH3C
(R)
O
O
OHH
(S)
H3N
HH3C
(R)
separate(R,R)-salt (S,R)-salt
OH
O
HO H(R)-Acid
HO
O
OHH(S)-Acid
H3O+ H3O
+
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Ch. 20 - 27
4. Preparation of Amines
4A.4A. Through Nucleophilic Substitution Through Nucleophilic Substitution ReactionsReactions
Alkylation of ammonia
XNH3
NH2
H
X
NH3
NH2
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Ch. 20 - 28
NH2 N
H X
X H
(over-alkylation)
NH3
N
HNH3
X
N N+
X
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Ch. 20 - 29
N N NNaN3
Alkylation of azide ion and reduction
X
NH2
Na/EtOHorLiAlH4
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Ch. 20 - 30
The Gabriel synthesis
N
O
O
H1. KOH
2.Br
N
O
O
NH2NH2EtOH, heat
N
N
O
O
H
H
H2N +
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Ch. 20 - 31
Alkylation of 3o amines
N
R
R
R Br+
(SN2)
N
R
R
R Br
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Ch. 20 - 32
4B.4B. Preparation of Aromatic Amines Preparation of Aromatic Amines through Reduction of Nitro through Reduction of Nitro CompoundsCompounds
R
H
R
NO2
R
NH2HNO3
H2SO4
H2, catalyst
1. Fe, HCl2. NaOH
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Ch. 20 - 33
4C.4C. Preparation of Primary, Secondary,Preparation of Primary, Secondary,and Tertiary Amines through Reductive and Tertiary Amines through Reductive AminationAmination
O
R R'
aldehydeor
ketone
NH3
[H]
N
R R'H
H H
1o amine
R"NH2
[H]
N
R R'H
H R"
2o amine
R"R"'NH
[H]
N
R R'H
R"' R"
3o amine
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Ch. 20 - 34
O
R R'H2N R"+
Mechanismtwo
steps
R R'
HO NHR"
Hemiaminal
R R'
NR"(- H2O)
Imine
[H]
NHR"
R R'H
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Ch. 20 - 35
(1) O NH2
NH3, H2/Ni
heat &pressure
Examples
(2)
O NH
1.
2. NaBH3CN
NH2
(3)O N
NH
1.
2. LiBH3CN
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Ch. 20 - 36
4D.4D.Preparation of Primary, Secondary, Preparation of Primary, Secondary, or Tertiary Amines through or Tertiary Amines through Reduction of Nitriles, Oximes, Reduction of Nitriles, Oximes, and Amidesand Amides
R C N
H
CR N
OHor[H]
RCH2NH2
O
CR N
R'
R"
RCH2N
R'
R"
[H]
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Ch. 20 - 37
(1) Br C
CH2NH2
NNaCN
DMSO
Ra Ni
H2Oheat
Examples
(2)
O NOH
H2N OH Na
EtOH
NH2
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Ch. 20 - 38
Examples
(3)Cl
pyridine
NH
O
N
O
1. LiAlH42. H2O
N
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Ch. 20 - 39
4D.4D.Preparation of Primary Amines Preparation of Primary Amines through the Hofmann and Curtius through the Hofmann and Curtius RearrangementsRearrangements
O
R NH2
Br2, NaOH
H2OR NH2
+ NaBr + Na2CO3
Hofmann rearrangement
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Ch. 20 - 40
(1) NH2
O
Br2
NaOH
NH2
Examples
(2)
NH2
O
NH2Br2
NaOH
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Ch. 20 - 41
MechanismO
R N
H
HOH O
R N
H
Br Br O
R N
H
Br
HO
O
R NBr
O C NR (Hofmann
rearr.)(isocyanate)
HOO C
N
OH
R
O C
N
O
R
H
+ CO2H
NR
H OHR NH2
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Ch. 20 - 42
Curtius rearrangement
O
R Cl
NaN3O
R N N NO C N
R+ N2 (g)
heat
R NH2
H2O
CO2 (g) +
O
Cl 1. NaN3
2. heat3. H2O
NH2
e.g.
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Ch. 20 - 43
5. Reactions of Amines
H Cl+Et3N
Acid-base reactions
Et3N H + Cl
+ BrNH2
Alkylation
BrN
H
H
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Ch. 20 - 44
+N
H
Cl
O
Acylation
N
O(- HCl)
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Ch. 20 - 45
NH2 NH2 NH2
E
E
E+
Electrophilic aromatic substitution
NH2: powerful activating group, ortho-para director
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Ch. 20 - 46
5A.5A. Oxidation of AminesOxidation of Amines
R3N O
(a tertiaryamine oxide)
R3NH2O2 or
R OO
H
O
(per acid)
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Ch. 20 - 47
6. Reactions of Amines withNitrous Acid
Nitrous acid (HONO) is a weak, unstable acid
HCl(aq) + NaNO2(aq) HONO(aq) + NaCl(aq)
H2SO4(aq) + 2 NaNO2(aq)
2 HONO(aq) + Na2SO4(aq)
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Ch. 20 - 48
6A.6A. Reactions of Primary Aliphatic Reactions of Primary Aliphatic Amines with Nitrous AcidAmines with Nitrous Acid
1o aliphatic amine
R NH2
R N N X
NaNO2HX (HONO)
RX
alkyl halides
alcoholsH2O
- H+alkenes
(aliphatic diazonium salt)
(highly unstable)
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Ch. 20 - 49
6B.6B. Reactions of Primary Arylamines Reactions of Primary Arylamines with Nitrous Acidwith Nitrous Acid
N N
XNaNO2
HX
R
NH2
R
(arenediazonium salt)
(stable at <5oC)
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Ch. 20 - 50
H
NAr
H
N O
NAr
H
N OH
HONO + H3O+ + A:
Mechanism
H2O NO + H2O
+ 2 H2ON O
H
NAr
H
OH2
- H3O+
NAr
H
N OH A
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Ch. 20 - 51
- HA + HA
NAr N OH2
Mechanism (Cont'd)
NAr
H
N OH
A
NAr N OH- HA
+ HADiazohydroxide
NAr NNAr NH2O +
diazonium ion
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Ch. 20 - 52
6C.6C. Reactions of Secondary Reactions of Secondary Amines with Nitrous AcidAmines with Nitrous Acid
NaNO2
HCl, H2ON H N N O
N
H
N
NO
NaNO2
HCl, H2O
N-Nitroso-amines
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Ch. 20 - 53
6D.6D.Reactions of Tertiary Amines with Reactions of Tertiary Amines with Nitrous AcidNitrous Acid
NaNO2
HCl, H2O
8oC
N N N O
NaNO2
HCl, H2OEt3N + Et3N N O ClEt3NH Cl
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Ch. 20 - 54
7. Replacement Reactions of Arenediazonium Salts
N NHONO
0 - 5oC
R
NH2
R
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Ch. 20 - 55
7A.7A. Syntheses Using Diazonium SaltsSyntheses Using Diazonium Salts
NN
R
R
OHCu2O, Cu2-
H2O
R
ClCuCl
CuBr
R
Br
R
CNCuCN
KI
R
I
1. HBF4
2. heat
R
F
H3PO2, H2O
R
H
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Ch. 20 - 56
7B.7B. The Sandmeyer Reaction: The Sandmeyer Reaction: Replacement of the Diazonium Replacement of the Diazonium Group by -Cl, -Br, or -CNGroup by -Cl, -Br, or -CN
CuCl
15 - 60oC
HCl, NaNO2
H2O
0 - 5oC
N2Cl
CH3
NH2
CH3
CH3
Cl
+N2
o-Toluidine
o-Chlorotoluene(74-79% overall)
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Ch. 20 - 57
CuBr
100oC
HBr, NaNO2
H2O
0 - 10oC
N2BrNH2
Br
+N2
m-Chloroaniline
m-Bromochlorobenzene(70% overall)
Cl Cl
Cl
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Ch. 20 - 58
CuCN
90 - 100oC
HCl, NaNO2
H2Oroom temp.
N2Cl
NO2
NH2
NO2
NO2
Cl
+N2
o-Nitroaniline
o-Nitrobenzonitrile(65% overall)
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Ch. 20 - 59
7C.7C. Replacement by —IReplacement by —I
KIH2SO4, NaNO2
H2O
0 - 5oC
NO2NO2 NO2
+ N2
p-Nitroaniline p-Iodonitrobenzene(81% overall)
NH2 N2HSO4 I
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Ch. 20 - 60
7D.7D.Replacement by —FReplacement by —FCH3CH3
CH3
BF3 + N2 +
m-Toluidine
m-Fluorotoluene(69%)
NH2 N2BF4
F
(1) HONO, H+
(2) HBF4
m-Toluenediazoniumfluoroborate
(79%)
heat
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Ch. 20 - 61
7E.7E. Replacement by —OHReplacement by —OH
CH3 CH3
p-Toluenediazoniumhydrogen sulfate
p-Cresol(93%)
N2HSO4 OH
Cu2O
Cu2+, H2O
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Ch. 20 - 62
7F.7F. Replacement by Hydrogen: Replacement by Hydrogen: Deamination by DiazotizationDeamination by Diazotization
CH3CH3 CH3
N2 +
p-Toluidine 65%(from p-Toluidine)
NH2 HN NH2
O
O2
(1) Br2
(2) OH , H2OBrheat
H2SO4, NaNO2H2O, 0 - 5oC
H2O, 25oC
O
H3PO2
CH3
N2
Br
CH3
Br
m-Bromotoluene(85% from 2-bromo-
4-methylaniline)
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Ch. 20 - 63
8. Coupling Reactions of Arenediazonium Salts
N N X + Q
N N Q
(Q = NR2 or OH)
(azo dyes)
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Ch. 20 - 64
(1)
N2 Cl OH
+
NN
OH
NaOH
H2O, 0oC
(orange solid)
Examples
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Ch. 20 - 65
(2)
N2 Cl N
+
NN
N
NaOAc
H2O, 0oC
(yellow solid)
Me
Me
Me
Me
Examples
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Ch. 20 - 66
(3)
N2 Cl OH
+
NN
NaOHH2O
Me
HO
Me
Examples
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Ch. 20 - 67
9. Reactions of Amines with Sulfonyl Chlorides
+
R"
NR' H Cl S Ar
O
O
R"
NR' S Ar
O
O
+ HCl
1. H3O+, heat
2. NaOH
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Ch. 20 - 68
9A.9A. The Hinsberg TestThe Hinsberg Test
Sulfonamide formation is the basis for a chemical test, called the Hinsberg test, that can be used to demonstrate whether an amine is primary, secondary, or tertiary
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Ch. 20 - 69
1o Amine
+
H
NR H Cl S
O
O
H
NR S
O
O
H
NR S
O
O
OH
(-HCl)
HClNR S
O
O
K
water insoluable(precipitate)
water-soluable salt(clear solution)
KOH
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Ch. 20 - 70
2o Amine
+
R2
NR1 H Cl S
O
O
R2
NR1 S
O
O
OH
(-HCl)
water insoluable(precipitate)
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Ch. 20 - 71
3o Amine
+
R2
NR1 R3 Cl S
O
O
R2
NR1 R3
NaOH
H3O+
water soluable
No apparentchange
H
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Ch. 20 - 72
10.Synthesis of Sulfa Drugs
NH2
O
HNO
O2
O
HN
SO2Cl
2 HOSO2Cl
80oC
H2N R
(-HCl)
O
HN
SO2NHR
NH2
SO2NHR
1. dilute HCl, heat
2. HCO3
(-H2O)
Aniline Acetanilide
Sulfanilamide
p-Acetamidobenzene-sulfonyl chloride
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Ch. 20 - 73
11.Analysis of Amines
11A.11A. Chemical AnalysisChemical Analysis Dissolve in dilute aqueous acid Moist pH paper
basic Hinsberg test 1o aromatic amines
azo dye formation with 2-naphthol
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Ch. 20 - 74
11B.11B. Spectroscopic AnalysisSpectroscopic Analysis IR
●1o amines 3300 – 3555 cm-1 (N–H)
two bands●2o amines
3300 – 3555 cm-1 (N–H) one band only
●3o amines No bands at 3300 – 3555
cm-1 region
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Ch. 20 - 75
●Aliphatic amines 1020 – 1220 cm-1 (C–N)
●Aromatic amines 1250 – 1360 cm-1 (C–N)
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Ch. 20 - 76
1H NMR spectra● 1o and 2o amines
N–H (0.5 – 5 ppm), usually broad, exact position depends on the solvent, concentration, purity and temperature
● N–H protons are not usually coupled to protons on adjacent carbons
● Protons on the carbon of an aliphatic amine are deshielded by the electron-withdrawing effect of the nitrogen and absorb typically in the 2.2–2.9 region
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Ch. 20 - 77
● Protons on the carbon are not deshielded as much and absorb in the range 1.0–1.7
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Ch. 20 - 78
13C NMR spectra
NH223.0 34.0
14.3 29.7 42.5
13C NMR chemical shifts ()
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Ch. 20 - 79
Mass spectra● The molecular ion in the mass
spectrum of an amine has an odd number mass (unless there is an even number of nitrogen atoms in the molecule)
● The peak for the molecular ion is usually strong for aromatic and cyclic aliphatic amines but weak for acyclic aliphatic amines
● Cleavage between the and carbons of aliphatic amines is a common mode of fragmentation
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Ch. 20 - 80
12.Eliminations Involving Ammonium Compounds
12A.12A. The Hofmann EliminationThe Hofmann Elimination
H
NR3
A quaternaryammoniumhydroxide
OH
HOH
+
heat
NR3
+
An alkene
A tertiaryamine
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Ch. 20 - 81
A quaternaryammonium
halide
RNMe3X
Ag2O
H2O
+ 2 AgX
A quaternaryammoniumhydroxide
RNMe3HO
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Ch. 20 - 82
Although most eliminations involving neutral substrates tend to follow the Zaitsev rule, eliminations with charged substrates tend to follow what is called the Hofmann rule and yield mainly the least substituted alkene 75%Br
+ NaBr + EtOH+EtONa
EtOH
25oC25%
5%NMe3
+ NMe3 + H2O+ OH
150oC95%
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Ch. 20 - 83
H
NMe3
Carbanion-liketransition state
(gives Hofmann orientation)
HO
H
Br
HO
Alkene-liketransition state
(gives Zaitsev orientation)
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Ch. 20 - 84
12B.12B. The Cope EliminationThe Cope Elimination
+N
Me
O150oCMe
R
H
RO N
H
Me
Me
A tertiaryamine oxide
An alkene N,N-Dimethyl-hydroxylamine
H
N
O
e.g.
heatN OH+
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Ch. 20 - 85
13.Summary of Preparations and Reactions of Amines
Preparation of amines
R NH2
N
O
O
H
1. KOH2. R-X3. NH2NH2, EtOH, heat
R Br
1. NaN32. LiAlH4
R Br
NH3R NO2
H2, cat. or1. Fe, HCl2. NaOH
O
R1 R2R =
R1 R2
NH3[H]
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Ch. 20 - 86
R NH2
N
R1 R2R =
R1 R2
OH
NaEtOH
1. LiAlH42. H2O
C NR
O
R NH2
1. LiAlH42. H2O
(R = R1CH2)
O
R NH2
Br2NaOH
1. NaN32. heat3. H2O
O
R Cl
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Ch. 20 - 87
Reactions of amines
R NH2
H X
RNH3 X
R N
H
S
O
O
Ar
ClS
O
O
Ar1. , NaOH
2. HCl
O
R' Cl
O
R'NR
base
H
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Ch. 20 - 88
Ar NH2
N2
Q
NN
Q
(Q = NR2 or OH)
HONO
0-5oCAr N2
Ar OHH2O
Cu2O, Cu2+
Ar ClCuCl
Ar BrCuBr
Ar CNCuCN
Ar IKI
Ar F1. HBF4
2. heat
Ar HH3PO2
H2O
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Ch. 20 - 89
H
NR3
+ H2O + NR3heat
OH+
Hofmann Elimination
Cope Elimination
NMe
H OMe
syn elimination
heat
MeN
Me
OH
+
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Ch. 20 - 90
END OF CHAPTER 21