22.16 nitrosation of alkylamines. nitrite ion, nitrous acid, and nitrosyl cation h+ –o no o no h...
DESCRIPTION
Nitrosyl Cation and Nitrosation + NOTRANSCRIPT
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22.1622.16Nitrosation of AlkylaminesNitrosation of Alkylamines
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Nitrite Ion, Nitrous Acid, and Nitrosyl CationNitrite Ion, Nitrous Acid, and Nitrosyl Cation
HH++––
OO••••••••
••••NN OO
•••• ••••••••
OO•••• ••••
NN OO•••• ••••
••••HH
HH++
OO••••NN OO
•••• ••••
HH
HH
++••••++
••••NN OO
•••• ••••++OO ••••
HH
HH
••••
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Nitrosyl Cation and NitrosationNitrosyl Cation and Nitrosation
++••••NN OO
•••• ••••
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Nitrosyl Cation and NitrosationNitrosyl Cation and Nitrosation
++••••NN OO
•••• ••••++••••NN
NN••••NN OO
•••• ••••++
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Nitrosation of Secondary AlkylaminesNitrosation of Secondary Alkylamines
++••••NN OO
•••• ••••++
NN••••NN OO
•••• ••••++
••••NN
HH
HH++HH
++
NN••••NN OO
•••• ••••••••
nitrosation of nitrosation of secondary amines secondary amines gives an gives an NN-nitroso -nitroso amineamine
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ExampleExample
(CH(CH33))22NHNH•••• NaNONaNO22, HCl, HCl
HH22OO(88-90%)(88-90%)
••••(CH(CH33))22NN
••••NN OO
•••• ••••
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Some N-Nitroso AminesSome N-Nitroso Amines
NN-nitrosopyrrolidine-nitrosopyrrolidine(nitrite-cured bacon)(nitrite-cured bacon)
NN-nitrosonornicotine-nitrosonornicotine(tobacco smoke)(tobacco smoke)
NN
NNOO
NN
NNOONN
(CH(CH33))22NN NN OO NN-nitrosodimethylamine-nitrosodimethylamine(leather tanning)(leather tanning)
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Nitrosation of Primary AlkylaminesNitrosation of Primary Alkylamines
++
NN••••NN OO
•••• ••••++
HH++HH
++
NN••••NN OO
•••• ••••••••
analogous to analogous to nitrosation of nitrosation of secondary amines secondary amines to this pointto this point
++••••NN OO
•••• ••••••••NN
HH
HHRR
HHRR RR
HH
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Nitrosation of Primary AlkylaminesNitrosation of Primary Alkylamines
NN••••NN OO
•••• ••••••••
this species reacts furtherthis species reacts further
RR
HH
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Nitrosation of Primary AlkylaminesNitrosation of Primary Alkylamines
NN••••NN OO
•••• ••••••••
RR
HH
HH ++
NN••••NN OO
••••••••
RR
HH HH
++
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Nitrosation of Primary AlkylaminesNitrosation of Primary Alkylamines
NN••••NN OO
••••••••
RR
HH HH
++
••••NN••••NN OO
••••••••
RR
HHHH
++
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Nitrosation of Primary AlkylaminesNitrosation of Primary Alkylamines
++••••NN
••••NN OO
••••••••
RR
HH
HHHH ++
••••NN••••NN OO••••
RR
HH
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Nitrosation of Primary AlkylaminesNitrosation of Primary Alkylamines
++
HH
••••NN••••NN OO••••
RR
HH
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Nitrosation of Primary AlkylaminesNitrosation of Primary Alkylamines
++
HH
••••NN••••NN OO••••
RR
HH
++NN NN ••••RR
HH
••••OO
HH
••••++nitrosation of a nitrosation of a primary alkylamine primary alkylamine gives an alkyl gives an alkyl diazonium iondiazonium ionprocess is called process is called diazotizationdiazotization
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Alkyl Diazonium Ions Alkyl Diazonium Ions
++NN NN ••••RR
alkyl diazonium ions alkyl diazonium ions readily lose Nreadily lose N22 to to give carbocationsgive carbocations
RR++ ++ NN NN ••••••••
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Example: Nitrosation of 1,1-DimethylpropylamineExample: Nitrosation of 1,1-Dimethylpropylamine
HH22OO
NHNH22
OHOH
++
NN NN++
HONOHONO
++
(80%)(80%)
(2%)(2%)(3%)(3%)
– – NN22
Fig. 22.5 (p 890)Fig. 22.5 (p 890)
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There is no useful chemistry associated with the There is no useful chemistry associated with the nitrosation of tertiary alkylamines.nitrosation of tertiary alkylamines.
Nitrosation of Tertiary Alkylamines Nitrosation of Tertiary Alkylamines
••••NNRR
RR
RR
NN••••NN OO
•••• ••••++RR
RR
RR
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22.1722.17Nitrosation of ArylaminesNitrosation of Arylamines
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reaction that occurs is reaction that occurs is electrophilic aromatic substitutionelectrophilic aromatic substitution
Nitrosation of Tertiary ArylaminesNitrosation of Tertiary Arylamines
(95%)(95%)
N(CHN(CH22CHCH33))221. NaNO1. NaNO22, HCl,, HCl,
H H22O, 8°CO, 8°C
2. HO2. HO––
N(CHN(CH22CHCH33))22
NNOO
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similar to secondary alkylamines;similar to secondary alkylamines;
gives gives NN-nitroso amines-nitroso amines
Nitrosation of N-AlkylarylaminesNitrosation of N-Alkylarylamines
(87-93%)(87-93%)
NaNONaNO22, HCl,, HCl,HH22O, 10°CO, 10°C
NHCHNHCH33
NCHNCH33
NN OO
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Nitrosation of Primary ArylaminesNitrosation of Primary Arylamines
gives aryl diazonium ionsgives aryl diazonium ions
aryl diazonium ions are much more stable thanaryl diazonium ions are much more stable thanalkyl diazonium ionsalkyl diazonium ions
most aryl diazonium ions are stable under the most aryl diazonium ions are stable under the conditions of their formation (0-10°C) conditions of their formation (0-10°C)
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Nitrosation of Primary ArylaminesNitrosation of Primary Arylamines
gives aryl diazonium ionsgives aryl diazonium ions
aryl diazonium ions are much more stable thanaryl diazonium ions are much more stable thanalkyl diazonium ionsalkyl diazonium ions
most aryl diazonium ions are stable under the most aryl diazonium ions are stable under the conditions of their formation (0-10°C) conditions of their formation (0-10°C)
ArNArN NN++
RNRN NN++ fastfast
slowslow
RR++ ++ NN22
ArAr++ ++ NN22
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Example:Example:
(CH(CH33))22CHCH NHNH22
NaNONaNO22, H, H22SOSO44
HH22O, 0-5°CO, 0-5°C
(CH(CH33))22CHCH NN NN++
HSOHSO44––
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Synthetic Origin of Aryl Diazonium SaltsSynthetic Origin of Aryl Diazonium Salts
ArAr HH
ArAr NNOO22
ArAr NNHH22
ArAr NN NN++
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22.1822.18Synthetic Transformations of Aryl Synthetic Transformations of Aryl
Diazonium SaltsDiazonium Salts
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Transformations of Aryl Diazonium SaltsTransformations of Aryl Diazonium Salts
ArAr NN NN++
ArAr HH
ArAr OHOH
ArAr II
ArAr FF
ArAr BrBrArAr ClCl
ArAr CNCN
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Preparation of PhenolsPreparation of Phenols
ArAr NN NN++
ArAr OHOH
HH22O, heatO, heat
hydrolysis of a diazonium salthydrolysis of a diazonium salt
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ExampleExample
2. H2. H22O, heatO, heat
(CH(CH33))22CHCH NNHH22
1. NaNO1. NaNO22, H, H22SOSO44
HH22O, 0-5°CO, 0-5°C
(CH(CH33))22CHCH OOHH
(73%)(73%)
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Transformations of Aryl Diazonium SaltsTransformations of Aryl Diazonium Salts
ArAr NN NN++
ArAr HH
ArAr OHOH
ArAr II
ArAr FF
ArAr BrBrArAr ClCl
ArAr CNCN
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Preparation of Aryl IodidesPreparation of Aryl Iodides
ArAr NN NN++
ArAr II
reaction of an aryl diazonium salt with reaction of an aryl diazonium salt with potassium iodidepotassium iodide
KIKI
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ExampleExample
2. KI, room temp.2. KI, room temp.
1. NaNO1. NaNO22, HCl, HCl
HH22O, 0-5°CO, 0-5°C
(72-83%)(72-83%)
NNHH22
BrBr
II
BrBr
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Transformations of Aryl Diazonium SaltsTransformations of Aryl Diazonium Salts
ArAr NN NN++
ArAr HH
ArAr OHOH
ArAr II
ArAr FF
ArAr BrBrArAr ClCl
ArAr CNCN
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Preparation of Aryl FluoridesPreparation of Aryl Fluorides
ArAr NN NN++
ArAr FF
heat the tetrafluoroborate salt of a diazonium ion;heat the tetrafluoroborate salt of a diazonium ion;process is called the Schiemann reactionprocess is called the Schiemann reaction
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ExampleExample
(68%)(68%)
NNHH22
CCHCCH22CHCH33
OO
2. HBF2. HBF44
1. NaNO1. NaNO22, HCl,, HCl,
HH22O, 0-5°CO, 0-5°C
3. heat3. heat
FF
CCHCCH22CHCH33
OO
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Transformations of Aryl Diazonium SaltsTransformations of Aryl Diazonium Salts
ArAr NN NN++
ArAr HH
ArAr OHOH
ArAr II
ArAr FF
ArAr BrBrArAr ClCl
ArAr CNCN
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Preparation of Aryl Chlorides and BromidesPreparation of Aryl Chlorides and Bromides
ArAr NN NN++
ArAr BrBrArAr ClCl
aryl chlorides and aryl bromides are prepared by aryl chlorides and aryl bromides are prepared by heating a diazonium salt with copper(I) chloride or heating a diazonium salt with copper(I) chloride or bromidebromidesubstitutions of diazonium salts that use copper(I) substitutions of diazonium salts that use copper(I) halides are called halides are called SandmeyerSandmeyer reactionsreactions
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ExampleExample
(68-71%)(68-71%)
NNHH22
NONO22
2. CuCl, heat2. CuCl, heat
1. NaNO1. NaNO22, HCl,, HCl,
HH22O, 0-5°CO, 0-5°C
ClCl
NONO22
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ExampleExample
(89-95%)(89-95%)
2. CuBr, heat2. CuBr, heat
1. NaNO1. NaNO22, HBr,, HBr,
HH22O, 0-10°CO, 0-10°CNNHH22
ClCl
BrBr
ClCl
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Transformations of Aryl Diazonium SaltsTransformations of Aryl Diazonium Salts
ArAr NN NN++
ArAr HH
ArAr OHOH
ArAr II
ArAr FF
ArAr BrBrArAr ClCl
ArAr CNCN
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Preparation of Aryl NitrilesPreparation of Aryl Nitriles
ArAr NN NN++
ArAr CNCN
aryl nitriles are prepared by heating a diazonium aryl nitriles are prepared by heating a diazonium salt with copper(I) cyanidesalt with copper(I) cyanidethis is another type of Sandmeyer reactionthis is another type of Sandmeyer reaction
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ExampleExample
(64-70%)(64-70%)
2. CuCN, heat2. CuCN, heat
1. NaNO1. NaNO22, HCl,, HCl,
HH22O, 0°CO, 0°CNNHH22
CHCH33
CNCN
CHCH33
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Transformations of Aryl Diazonium SaltsTransformations of Aryl Diazonium Salts
ArAr NN NN++
ArAr HH
ArAr OHOH
ArAr II
ArAr FF
ArAr BrBrArAr ClCl
ArAr CNCN
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Transformations of Aryl Diazonium SaltsTransformations of Aryl Diazonium Salts
ArAr NN NN++
ArAr HH
hypophosphorous acid (Hhypophosphorous acid (H33POPO22) reduces diazonium ) reduces diazonium salts; ethanol does the same thingsalts; ethanol does the same thingthis is called this is called reductive deaminationreductive deamination
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ExampleExample
(70-75%)(70-75%)
NaNONaNO22, H, H22SOSO44,,
HH33POPO22
NNHH22
CHCH33 CHCH33
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Value of Diazonium SaltsValue of Diazonium Salts
1) 1) allows introduction of substituents such as allows introduction of substituents such as OH, F, I, and CN on the ringOH, F, I, and CN on the ring
2) 2) allows preparation of otherwise difficultly allows preparation of otherwise difficultly accessible substitution patternsaccessible substitution patterns
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NNHH22
BrBr
BrBr
BrBr
ExampleExample
(74-77%)(74-77%)
NaNONaNO22, H, H22SOSO44,,HH22O, CHO, CH33CHCH22OHOH
NNHH22
BrBr22
HH22OO
(100%)(100%)
BrBr
BrBrBrBr
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22.1922.19Azo CouplingAzo Coupling
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Azo CouplingAzo Coupling
Diazonium salts are weak electrophiles.Diazonium salts are weak electrophiles.React with strongly activated aromatic React with strongly activated aromatic compounds by electrophilic aromatic compounds by electrophilic aromatic substitution.substitution.
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Azo CouplingAzo Coupling
Diazonium salts are weak electrophiles.Diazonium salts are weak electrophiles.React with strongly activated aromatic React with strongly activated aromatic compounds by electrophilic aromatic compounds by electrophilic aromatic substitution.substitution.
ArAr NN NN++
Ar'Ar' HH++ ArAr NN NN Ar'Ar'
an azo compoundan azo compound
Ar' Ar' must bear a strongly electron-releasing group must bear a strongly electron-releasing group such as OH, OR, or NR such as OH, OR, or NR22..
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ExampleExample OHOH
++ CC66HH55NN NN++
OHOH
NN NCNC66HH55
ClCl––