Dr. Wolf's CHM 201 & 202 11-1 Chapter 11 Arenes and Aromaticity.
Chapter 6 Arenes and Aromaticity 6.1 The Structure of Benzene 1. A resonance theory 2. An orbital...
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Transcript of Chapter 6 Arenes and Aromaticity 6.1 The Structure of Benzene 1. A resonance theory 2. An orbital...
![Page 1: Chapter 6 Arenes and Aromaticity 6.1 The Structure of Benzene 1. A resonance theory 2. An orbital hybridization view 3. The molecular obitals 6.2 Nomenclature.](https://reader037.fdocuments.in/reader037/viewer/2022102606/56649e3f5503460f94b2f8e0/html5/thumbnails/1.jpg)
Chapter 6 Arenes and Aromaticity6.1 The Structure of Benzene 1. A resonance theory 2. An orbital hybridization view 3. The molecular obitals6.2 Nomenclature of Benzene Derivatives6.3 Aromaticity and the Huckel(4n + 2)rule 6.3.1 Annulenes( 轮烯 ) 6.3.2 Aromatic ions 6.3.3 Polycyclic aromatic hydrocarbons6.4 Reactions of Arenes 6.4.1 Aromatic ring as a substituent 1. Halogenation of α - H of arenes
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2. Oxidation of Alkylbenzenes 3. Addition Reaction of Alkenylbenzenes6.4.2 Aromatic Ring as a Functional Group: Electrophilic Aromatic Substitution6.4.3 Halogenation of Benzene6.4.4 Nitration of Benzene6.4.5 Sulfonation of Benzene6.4.6 Friedel-Crafts Alkylation of Benzene6.4.7 Friedel-Crafts Acylation of Benzene Clemmensen reduction Wolff-Kishner reduction
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6.4.8 Effects of Substituents on Reactivity and Orientation 6.4.8.1 Classification of Substituents 6.4.8.2 Substituent Effects in Electrophilic Aromatic Substitution6.4.9 Multiple Substituent Effects6.4.10 Synthetic Applications
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Organic compoundsAliphatic
Aromatic
脂肪族芳香族
Aromatic compound: Benzene
C6H6
Fragrant:
A low ratio hydrogen / carbon.
Balsams( 香脂 )
C
O
H
Benzaldehyde
oil of bitteralmond
COOH
Benzoic acid
CH3
TolueneTolu balsam
Estrone 雌激素酮
CH3CHCH2
CH3
CHCOOH
CH3Ibuprofen 布洛芬
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6.1 Structure of BenzeneThree modern theories:1. A resonance theory( 共振论 )1. A resonance theory( 共振论 )
The structure of benzene is planar: regular hexagon( 正六边型 ).The bond angles: 120 °The C–C bond lengths : 1.39Åsp2–sp2 single bond: 1.46Åsp2–sp2 double bond: 1.34A hybrid of the two Kekulé structures:
is equivalent to
Cyclic conjugation in benzene leads to a great stability.
P153,5.3P153,5.3
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C C
CCCC HH
H H
2. An orbital hybridization view2. An orbital hybridization view In a mole. of benzene, all C atoms aresp2–hybridized.6 C–C σ bonds: sp2–sp2 overlap,6 C –H σ bonds: sp2–1s overlap.
The 6 2p orbitals thatare perpendicular to the σ frameworkoverlap to form πorbital.
The 6 π electrons aredelocalized over all six C.
Resonanceenergy:152 kJ/mol
Resonanceenergy:152 kJ/mol
A closed π conjugate system.
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3. The molecular obitals3. The molecular obitals The 6 overlapping 2p obitals combine to form a set of 6 π molecular orbitals:
Antibonding orbitals
Bonding orbitals
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6.2 Nomenclature of Benzene Derivatives 1. Monosubstituted benzenes A. Benzene as the parent name.
CH3
Toluene( 甲苯 )
Cl
Chlorobenzene( 氯苯 ) Isopropylbenzene
CHCH3
CH3
NO2
Nitrobenzene( 硝基苯 )
B. Benzene as a substituentC6H5–, Ph–: phenyl.
PhC CH
Phenylacetylene( 苯乙炔 )
PhC
CH3
CHCH3
2-Phenyl-2-butene
CH2
Diphenylmethane
CH2 Cl
Benzylchloride( 苄基氯 )
P154,5.4P154,5.4
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2. Disubstituted benzenesThree isomers:
1,2-Dibromobenzeneo-Dibromobenzene
ortho-
Br
Br
Br
Br1,3-m-
meta-
Br
Br1,4-p-
para-CH3CH3
o-Xylene(0- 二甲 苯 )
3. Polysubstituted Benzenes
2-Chloro-1,4-dinitrobezene
ClNO2
NO2
(1,4- 二硝基 -2- 氯苯 )
CH3
CH3H3C
1,3,5-Trimethylbezene( 均三甲苯 )
Common name:P155
Common name:P155
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6.3 Aromaticity and the Huckel (4n + 2) rule
Aromaticity: a special stability.On the basis of the calculation by MO. Theory,
Huckel (4n + 2) rule:a. The monocyclic and fully conjugated polyenes.
Ch.276 Ch.276
b. All atoms in the ring are coplanar.c. The Mole. possesses(4 n+2) π electrons.
6.3.1 Annulenes( 轮烯 )
cyclobutadieneπ electrons 4
[4]-Annulene[6]-Annulene
cyclooctatetraene[8]-Annulene
Tub-mole.
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Eric Hückel
1896
"Eric Hückel received his PhD in experimental Physics in 1921 at the University of Göttingen. After spending a year with David Hilbert in mathematics and Max Born, he left Göttingen for a position at the ETH Federal Institute of Technology in Zurich with Peter Debye. While at Zurich, Hückel and Debye developed the Debye-Hückel theory of strongelectrolytes. In 1930 Hückel received an appointment in chemical physics at the Technical Institute in Stuttgart. In 1937 he was appointed a professor of theoreticalphysics at the University of Marburg, where he remained until his retirement in 1962." (Source: DA McQuarrie "Quantum Chemistry", University Science Books, 1983) In the quantum chemistry community, Hückel is best known for introducing in 1930a simple theory for the treatment of conjugated molecules and aromatic molecules.This theory came to be known as"Hückel molecularorbital theory" or simply"Hückel Theory". This was later extended by Roald Hoffmannand has been widely used in organic and inorganic chemistry.
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HH
Cyclodecapentaene( 环癸五烯 )
6.3.2 Aromatic ions
H Hstrongbase
H CH2: sp3 sp2cyclopentadieneCyclopentadienyl
anion π electrons: 6
H HCycloheptatriene
( 环庚三 烯 )Cycloheptatrienyl
cation
H
H Ch.P278Ch.P278
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6.3.3 Polycyclic aromatic hydrocarbonsP279P279
Naphthalene( 萘 )
Anthracene( 蒽 )
Phenanthrene( 菲 )
12
345
6
78 1
2
345
6
78 9
10 56
7
1
2
34
8
9 10
The hybrid of three resonance forms
• following Hückel rule• Aromaticity
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6.4 Reactions of Arenes6.4.1 Aromatic ring as a substituent
CH3Cl2h
CH2ClCl2h
CHCl2Cl2h
CCl3Ex.
1. Halogenation of α - H of arenes
CH2CH3 + N
O
O
Br PhCOOCPh
O O
CCl4, 80 C°CHCH3
Br
+ N
O
O
H
Ethylbenzene N-BromosuccinimideN- 溴代丁二酰亚胺
(NBS)
(87%)
Allylic halogenation:Allylic halogenation:CH3 CH CH2
NBSh,CCl4
CH2 CH CH2
Br
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2. Oxidation of Alkylbenzenes P170,5.11P170,5.11
The alkyl side chain with α - H on a benzene ring is oxidized to benzoic acid by chromic acid( 铬酸 ) or KMnO4:
(86%)
t-Butylbenzene
CH2CH2RNa2Cr2O4
H2O,H2SO4,heatCOOH
CH3
NO2
Na2Cr2O4
H2O,H2SO4,heat
COOH
NO2
C
CH3
CH3CH3
Na2Cr2O4
H2O,H2SO4,heatNO reaction
Oxidant:KMnO4
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3. Addition Reaction of Alkenylbenzenes6.4.2 Aromatic Ring as a Functional Group: Electrophilic Aromatic Substitution
( 芳环上的亲电取代反应 ) P157 P157
When the aromatic ring of benzene reacts with a electrophilic reagent, the substitutionreaction occurs: A benzene ring with
6 π electrons in a cyclic conju-gated system is a site of electron-rich.
+ E Y
+ YHE
+ E Y
+ YHE
Electron donor: benzene ringElectron acceptor: E+, a Lewisacid.
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Aromatic electrophilic substitution reactions: The electrophlic part of a reagent replaces a hydrogen atom from aromaticring.
Figure 1 Types of electrophilic aromatic substitution of benzeneFigure 1 Types of electrophilic aromatic substitution of benzene
HHalogenationHalogenation
NO2
NitrationNitration SO3H
SulfonationSulfonation
R
AlkylationAlkylation
Acylation( 酰基化 )
Acylation( 酰基化 )
C
O
RXP157P157
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H+ Br2
Feheat
Br+ HBr
(75%)The Lewis acids most commonly used are FeCl3, FeBr3 and AlCl3.
2Fe + 3X2 2FeX3
The mechanism for bromination of benzene:Step 1 Polarization of Br2.
Br Br + FeBr3 Br FeBr3
BrBr Br + FeBr3 Br FeBr3
Br
The formation of the bromine-iron(III)bromide complex.
6.4.3 Halogenation of Benzene
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Step 2 The attack of polarized bromine to benzene ring .
+ Br FeBr3
Br
BrH + Br FeBr3
slow
The formation of nonaromatic carbocation.Allylic cation: p- π conjugation
Delocalization of π - electrons generatesthe resonance forms:
BrH
BrH
BrH
BrH
BrH
BrH
Step 2 is rate-determining.Step 3 The loss of a proton to restore the aromatic system.
BrH + Br FeBr3
Br+ FeBr3HBr +
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Step 1. Polarization of Br2.
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Step 2 The attack of polarized bromine to benzene ring .
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Step 3 The loss of a proton to restore the aromatic system.
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Reactivity : F2 > Cl2 > Br2 > I2 Iodination has to carry out in the presence of an oxidizing agent:
+ I2HNO3
I
Iodobenzene(86%)Ex.
6.4.4 Nitration( 硝化反应 ) of Benzene Aromatic rings can be nitrated by reaction with a mixture of concentratednitric acid and sulfuric acid:
+ HNO3H2SO4
50 - 55 C°
NO2+ H3O + HSO4
The generation of electrophile, E+:HNO3 + 2H2SO4 NO2 + H3O + 2HSO4
Nitronium ion( 硝 离子 )
Nitrobenzene(85%)
CH3NO2
NO2
O2N
Trinitrotoluene(TNT)
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6.4.5 Sulfonation( 磺化反应 ) of Benzene Benzene reacts with fuming sulfuric acid to produce benzene sulfonic acid:
H+ S
O
OO
25 C°
concd H2SO4
S
O
O
OH
Sulfur trioxide Benzenesulfonic acid ( 苯磺酸 )(56%)
Fuming H2SO4: a mixture of H2SO4 and SO3.
Mechanism of the reaction:
Step 1 Generation of the electrophile:
2H2SO4 SO3 + H3O + 2HSO4
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Step 2. Sulfur trioxide as a electrophile attacks benzene in the rate-determing step.
Step 3. The loss of a proton to restore the aromatic system.
Step 4. A rapid proton transfer to produce benzenesulfonic acid.
Sulfonation is favored in strong acid,Desulfonaton is favored in hot,dilute aqueous acid.
The sulfonation of benzene is reversible.The sulfonation of benzene is reversible.
SO3+ H2SO4
fastSO3H
HSO4+
H2N
SO O
NH2
Sulfanilamide( 磺胺 )SO3
H + HSO4fast SO3
+ H2SO4
H+ S
O
OO
slow SO3H An antibiotic
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6.4.6 Friedel-Crafts Alkylation of Benzene Benzene reacts with alkyl halide in the presence of AlCl3 as catalyst:
+ CH3CHCH3
Cl
AlCl3 CHCH3
CH3+ HCl
Cumene( 枯烯 )IsopropylbenzeneMechanism of the reaction:
Step 1. The formation of carbocation:
CH3
CHCH3
Cl + AlCl3CH3
CHCH3
+ Cl AlCl3
Step 2. The carbocation as a electrophile attacks benzene ring, a C–C bond is formed:
H+
CH3
CH
CH3
slow CHCH3H
CH3
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CHCH3H
CH3
+ Cl AlCl3fast CHCH3
CH3
+ HCl + AlCl3
• CH3X and RCH2X do not form the carbocation, they form the complex:
RCH2 X AlX3
• The rearrangement can occur when especially a primary halides are used:
H+ (CH3)2CHCH2Cl
AlCl30 C°
C(CH3)3 + HCl
(66%)
Step 3. Loss of a proton to produce the alkylbenzene
CCH3
CH3
CH2
H
Cl AlCl3 CCH3
CH3
CH3 + Cl AlCl3
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• Friedel-Crafts alkylation can be availble to other systems that generate a carbocation:Ex.
A alkene and a acid.
A alcohol and a acid. (56%)
+H2SO4
+ HOBF3
60 C°
Cyclohexyl benzene(65%)
• Polyalkylation
Ch. P252 Ch. P252
+ (CH3)3CClAlCl3
C(CH3)3
+
C(CH3)3
C(CH3)3
+
Majorproduct
Minorproduct
Another limitation to alkylation on ring
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Charles Friedel (1832-1899) Charles Friedel was born inStrabourg, Frans,and studiedat the Sorbonne in Paris. He was among the first to attempt manufacture synthetic diamonds. He was professor of chemistry at the Sorbonne(1884-1889).
James Mason Crafts (1839-1917)James Mason Crafts was born in Boston, Massachusetts,and graduated from Harvard in 1858. He served as president in the Massachusetts Institute ofTechnology (1897-1900).
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6.4.7 Friedel-Crafts Acylation of Benzene ( 酰基化反应 ) Benzene reacts with a acyl halide ( 酰卤 ) in the presence of AlCl3, to produce a acylbenzene( 酰基苯 ).
H+ CH3C
O
ClAlCl3
80 C°excess benzene
CCH3
O
+ HCl
Acetophenone( 苯乙酮 )(97%)Reagents: Acyl chloride (or acid chloride):
80 C°CH3C
O
OH SOCl2+ CH3C
O
Cl + SO2 + HCl
Carboxylic acids react with thionyl chloride( 亚硫酰氯 ) or PCl5:
Carboxylic acid anhydrides( 酸酐 ):H
+ CH3C
O
O CCH3
OAlCl3
excess benzeneCCH3
O
+ CH3C
80 C°
O
OH
(83%)
Ch. P252Ch. P252
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• Limitation to Friedel-Crafts Reactions:• Limitation to Friedel-Crafts Reactions:Friedel-Crafts reactions do not occur when powerful electron-drawing groupsare present on the aromatic ring.
-NO2, -SO3H, RCO-,-COOH, -NR3 ect..+
AlCl3
NH2
+ R X NO reaction
NH2 + AlCl3 NH2 AlCl3
Preparation of unbranched alkyl benzene:
+ CH3CH2CH2CCl
OAlCl3 CCH2CH2CH3
O
+ HCl
• Application of acylation to aromatic ring• Application of acylation to aromatic ring
1-Pheny-1-butanone(1- 苯基 1- 丁酮 )(86%)
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Clemmensen reduction:Clemmensen reduction:
The ketone can be reduced to alkylbenzeneby refluxing with HCl containing amalgamated zinc( 锌汞齐 ):
C
OCH2
CCH2CH2CH3
OHCl
Zn(Hg)CH2CH2CH2CH3
Butylbenzene(73%)
Wolff-Kishner reduction:Wolff-Kishner reduction:Heating with hydrazine( 肼 ) and hydroxide
CCH2CH3
OH2NNH2,KOHtriethylene glycol
175 C°
CH2CH2CH3
1-Pheny-1-propanone(1- 苯基 -1- 丙酮 )
Propylbezene( 丙苯 )(82%)
HOCH2CH2OCH2CH2OCH2CH2OHTriethylene glycol( 三甘醇 or 三 缩 乙二醇 )
Ch.P355Ch.P355
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6.4.8 Effects of Substituents on Reactivity and Orientation
P164, 5.9P164, 5.9Y
To substituted benzenes: the substituent on the ring affects both the rate of the reaction and the site of attack.
Effect of substituents on the reactivity and orientation or regioselectivity.
Substituents can be classified into three groups:
1. Ortho and para Directing activators1. Ortho and para Directing activators(邻、对定位致活基团)
Substituents in first category( 第一类定位基团 )• Making the ring more reactive than benzene.
6.4.8.1 Classification of Substituents
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Hydroxyl groupis a activitor Hydroxyl groupis a activitor
OH H Cl NO2OH H Cl NO2
Relative rateof nitration 1000 1 0.033 6 × 10-8
Reactivity • Directing substitution primarily to the ortho and para position to themselves
CH3
HNO3
HOAc
CH3
NO2+
CH3
+
CH3
NO2
NO2
o- p- m-63% 34% 3%
2. Meta directing deactivators
• Making the ring less reactive than benzene.
( 间位定位致钝基团 )Substituents in second category( 第二类定位基团 )
Ex. –NO2, –CF3 etc.(et cetera[it´setr ])e
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• Directing substitution primarily to the meta position to themselves
CF3
HNO3
H2SO4
CF3
NO2+
CF3
+
CF3
NO2
NO2
6% 3% 91%
3. Ortho and para directing deactivators3. Ortho and para directing deactivators
–X: ClHNO3
H2SO4
ClNO2
+
Cl
+
Cl
NO2
NO2
30% 69% 1%
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X –I, +C
Ortho- andpara- directing
activitors
Ortho- andpara- directing
deactivitors
Meta-directing
deactivitors
FIGURE 6.1 Classification of substituent effects in electrophilic aromatic substitution.
OCH3 CH3NHCOCH3 Cl I C OR
OH(R)C C OH
O OSO3H C N
NH2 F Br NO2OH HO CF3 CCl3 NR3
6.4.8.2 Substituent Effects in electrophilic Aromatic substitution
Substituent Effects
P166P166
Meta-directingdeactivitors
Electron-withdrawing
Ortho- and para- directingactivitors
Electron-releasing
Reactivity
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1. Ortho and para directing activitorsActiviting effect:
CH3CH3
E
E
H
• Electron-releasing groups increase the density of electron cloud to favor electrophilic attack.
• stabilize the carbocation.Orientation effect:
OH
EH
EH
EH
OH OH OHEH
OH
Orthoattack
Paraattack
OH
EH
OH
EH
OH
EH
Metaattack
Most stableresonancestructure
Most stableresonancestructure
OH
E H
OH
E H
OH
E H
OH
HE
Para and orthoattacks are primary.
Para and orthoattacks are primary.
P168, P168,
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2. Meta directing deactivitorsDeactiviting effect:
CF3
E
CF3
EH
• Electron-drawing groups decrease the density of electron cloud of aromatic ring.• Making intermedias highly unstable
Orientation effect:
CF3
CF3EH
EH
EH
CF3 CF3
Orthoattack
EH
EH
EH
CF3 CF3 CF3
Paraattack
Metaattack
Most unstableintermeidate
Meta attack is primary
Meta attack is primary
E H E H HE
CF3 CF3 CF3
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3. HalogensX Halogen as a substituent on aromatic ring
possesses both electron-drawing inductiveeffect(-I) and electron-releasing conjugativeeffect(+C).
X -I > +C
OROH
NH2
-I < +C
Inductive effect of halo-groupdeactivates aromatic ring.
Halo-group stabilizes the inter-mediate relative to that from ortho and para attack deactivates aromatic ring by donating unshared pair of electrons in the same way as –OH.
Cl
E H
Cl
E H
Cl
E H
Cl
HE
Ch.P262Ch.P262
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6.4.9 Multiple Substituent Effects X
Y
Further electrophilic substitution of a disubstituted bezene is governed by Additivity( 累加性 ) of effects.
1. If the directing effects of the two groups reinforce( 增强 ) each other, there is no problem.
CH3
NO2
HNO3H2SO4
CH3
NO2
NO2
2. If the directing effects of the two groups are oppose each other, the more powerful activiting group has the dominant influence.
Ch. P266Ch. P266
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NHCH3
Cl
Br2HOAc
NHCH3
Cl
Br
CH3
COOHH2SO4
HNO3
CH3
COOHNO2
+
CH3
COOH
O2N
3. When two positions are comparably actived by alkyl group, substitution usually occurs at the less hindered site.
(88%)
CH3
CHCH3 CH3
HNO3
CH3
CHCH3 CH3
NO2
H2SO4
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6.4.10 Synthetic ApplicationsCh.172,5.13Ch.172,5.13Ex. 1
4-Chloro-1-nitro-2-propylbenzene(2- 丙基 -4- 氯硝基苯 )
NO2
Cl CH2CH2CH3
Cl
NO2
Cl
NO2
NO2 NO2
ClCl
m-ChloropropiophenoneSynthetic route:( 间 - 氯苯基乙基 ( 甲 ) 酮
( )
( )( )
Cl
NO2
( )( )
( )
O
( )( )
( )( )
CH3CH2CCl
O
AlCl3
OCl
Cl2
FeCl3
ClH2NNH2
KOHHNO3
H2SO4
Retrosynthetic analysisRetrosynthetic analysisO
Cl
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P178, 5.22 (a), (c)5.23 (c), (f)5.26 (b)5.275.28 (b) ( 苯基腈 或氰基苯 )5.32 (b) ( 邻 - 甲基苯酚 )5.33 (c)5.395.40 (b)5.41(b)5.425.445.45
P178, 5.22 (a), (c)5.23 (c), (f)5.26 (b)5.275.28 (b) ( 苯基腈 或氰基苯 )5.32 (b) ( 邻 - 甲基苯酚 )5.33 (c)5.395.40 (b)5.41(b)5.425.445.45
5.485.495.505.51
5.485.495.505.51
Chapter 6 to Problems