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Reactions of alkyl halides: Ar-X
1. SN2 NR
2. E2 NR
3. organo metallic compounds similar
4. reduction similar
Ag+
-OH
X -OR
-CN
C C X
vinyl halide ArH
AlCl3
Bond Lengths (Å)
C—Cl C—Br
CH3—X 1.77 1.91
C2H5—X 1.77 1.91 sp3
(CH3)3C—X 1.80 1.92
CH2=CH—X 1.69 1.86
sp2
C6H5—X 1.69 1.86
•In aryl halides, the carbon to which the halogen is attached
is sp2 hybridized.
•The bond is stronger and shorter than the carbon-halogen
bond in aliphatic compounds where the carbon is sp3
hybridized.
•Hence it is more difficult to break this bond that is why aryl
halides resist the typical nucleophilic substitution reactions
of alkyl halides.
•The same is true of vinyl halides where the carbon is also
sp2 hybridized and not prone to nucleophilic substitution.
•In a manner analogous to the phenols & alcohols, we have
the same functional group in the two families, aryl halides
and alkyl halides, but very different chemistries.
ARYL HALIDES REACTIONS:
1. Formation of Grignard reagent
2. EAS
3. Nucleophilic aromatic substitution -bimolecular displacement
(Ar must contain strongly electron withdrawing groups ortho
and/or para to X)
4. Nucleophilic aromatic substitution -elimination-addition
(Ring not activated to bimolecular displacement but strongly
basic nucleophiles are required)
1) Grignard Synthesis
Mg
Br MgBr
anhyd. Et2O
Mg
Cl MgCl
THF
2) Electrophilic Aromatic Substitution (EAS):
The –X group is electron-withdrawing and
deactivating in EAS, but is an ortho/para director.
Br Br Br
HNO3, H2SO4 NO2
+
Br NO2
SO3H
H2SO4,SO3
+ Br SO3H
Br Br
Br2,Fe Br
+
Br
Br
CH2CH3
CH3CH2-Br, AlCl3
+ Br CH2CH3
3) Nucleophilic aromatic substitution. Bimolecular Displacement
Ar must contain strongly electron withdrawing groups ortho
and/or para to the X.
Cl NH2
NO2 NO2
+ NH3
NO2 NO2
Br OCH3
O2N NO2 O2N NO2
+ NaOCH3
NO2 NO2
Cl
+ NaOH NR
OH
350oC, 4500 psi H+
Cl OH
15% NaOH, 160oC H+
NO2 NO2
Cl OH
O2N NO2 O2N NO2
warm water
NO2 NO2
Cl NH2
NH3, Cu2O, 200oC, 900 psi
Cl NH2
NO2 NH3, 170oC NO2
NO2 NO2
Cl NH3
O2N NO2 O2N NO2
NH3, room temp.
NO2 NO2
bimolecular displacement (nucleophilic aromatic substitution)
mechanism:
Z
1) X + :Z RDS
X
Z + :X
2) Z
X
Z
Z Z Z
X X X
Z Z
G
X X
G
+ NaNH2, NH3
F Li
H2O
+ Li
Elimination-Addition mechanism (nucleophilic aromatic
substitution)
X X
H :
1) + :NH2 + NH3
elimination
X
:
2) + :X
benzyne
:
NH2
3) + :NH2
addition
H
NH2
:
NH2
4) + NH3 + :NH2
While the concept of “benzyne” may appear to be strange,
there is much evidence that this mechanism is correct.
Cl NH2
NaNH2 NH2
* * + *
NH3
Br
H3C OCH3 NaNH2
NR
NH3
Cl Cl
D H
+ :NH2
benzyne intermediate has been trapped in a Diels-Alder
condensation: