lec51 thiophene 1 – 1,4 – dicarbonyl compound with a source of sulphur
TRANSCRIPT
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Thiophene
1 – 1,4 – dicarbonyl compound with a source of sulphur
OO R'RP2S5
OS R'R
R'R SH OH-H2O
SR'R
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2 – The Hinsberg Synthesis The consecutive aldol condensation between α 1,2 – dicarbonyl compound and diethylthiodiacetate give thiophenes .The immediate product is an ester – acid produced by a stobbe – type mechanism , but the reaction are often worked up via hydrolysis to offord an isolated diacid
CH3 - C - C - CH3 || || O O
+EtO2CCH2
SCH2CO2Et
EtO2C -C S
CH3-C C - CH3
C - O2C-Et
Cu
300 c0
EtO2C S
CH3CH3
-2H2O
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Chemical Reaction Reaction with electrophilic reagent take place at position 2 & 3 but at 2 take place much faster yield a stable product .
Nitration
S
HNO3
AC2O/ACOH 0 0C
S NO2
+
S
NO2
60% 10%Sulphonation
S
SO3-
N+
CH2Cl2
Ba(OH)2
S SO3
-
Ba2+2
86%
Use of the pyridine – sulfur trioxide complex is probably the best method
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Halogenation
S I
70 %
I2
aq.HNO3S
S BrBr
S Br
90 %
84 %
Br2/Et2O
48%HBr
-10 +10 0C
Br2/Et2O
48%HBr
-25 -5 0C
90 0C
Halogenation of thiophene occurs very readily at room temperatures and is rapid even at – 30 cº in the dark.
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Acylation
S S C || O
CH3
80%
MeCOCl
SnCl4
The Friedel – crafts acyalation of thiophene is much – used reaction and produced generally to give good yield under controlled condition , adding catalyst to thiophene and acylatting agent avoid reaction of aluminium chloride with thiophene to generate tars
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N
Indolizine
X
Iso indole Isobenzofuran
Isobenzothiophenes
X
Indole X = NHBenzofuran X = O
Benzo thiophene X = S
Reactivity of indoles, benzo[b]thiophenes, benzo[b]furans.isoindoles, benzo[c]thiophenes and isobenzofurans
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IndolesIndoles are colourless crystalline solids .Many simple indoles are available commercially and all of these are produced by synthesis .Most indoles are stable in air with exception of those which carry simple alkyl group at c – 2 autoxidises easily even in dark brown bottle.
The word indoles derived from the word India blue dye. chemical degradation of the dye give rise oxygenated indoles .which named indoxyl and oxindole ; indol as first prepared in 1866 by zinc dust distillation of oxindole
NH
O
Zndust
(Red)NH
Oxidndole Indole
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Indoles are widely distributed in nature Tryptophen is an essential amino acid
NH
COOH
NH2
tryptophan
The formula of indole was proposed by Baeyer in 1869 and was based on the synthesis outlined
CH2COOH
NO2
Fe , NaOH
fuse NH
CH2COOH
NH2
-H2O
NH O
red Sn , HCl Zn dust , disti
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The resonance energy of indole calculated from its heat of combustion is )47 – 49 ( kcal / mol the increase in resonance energy over pyrrole )23 – 27 ( is almost identical to the difference between the resonance energies of naphthalene )61( and benzene )36(
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Chemical properties The chemical properties of indole are quite similar of these of pyrrole
1 – The direct oxidation of indole .PhC2 O OH O3 , H2ONHRR'CORNHCOR'PhCO2OHO3 , H2ONHCOHNHCOHThe nitrogen containing ring of many substituted indoles can be
opened by the action of peroxy acid and ozone.
PhC 2 O OH
O3 , H 2ONH
R
R'
COR
NHCOR'
PhCO2OH
O3 , H 2ONH
COH
NHCOH
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2 – Addition reaction Indole , like pyrrole is very weak base and it is polymerized by acid giving crystalline dimmer
NH N
H
NH
indole dimer
Acid
3 – Reaction
NH N
H
2,3-dihdroindole
Zn
octa hydroindole
NH
sever
condition
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4 – Subistitution reactions the hydrogen at position 1 of indole is acidic and can be displaced by metallic sodium or pot . hydroxide at 125 – 130 c° or by Grignard reagent
NH
MeMgI
NMgI
HCOOEt
NH
CHO
2,3-dihdro indole
NCHO
Some
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Electrophilic subistitution
NH
..
NH
NH
+
E
E
NH
NH
SO3SO3
Pyridine
NH
Cl SOCl2
attack is more stable at position 3
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Electrophilic subistitution reaction NHEHH..NHEH..NHEHmore stablearomatic sextet preserved attack at position 2
The pyrrole ring in the indoles readily undergo subistitution reactions .The general Pattern of reaction is similar to that observed with Pyrrole itself except that many of reaction with indole introduce 3 – Subistituents , lead to 3-subistituted indoles .This orientation can be accounted as follows
NH
E
H
H
..NH
E
H
..NH
E
H
more stablearomatic sextet preserved
attack at position 2
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This orientation agreement with the calculated change destant for indole
NH
1.065
1.059
Gattermen reaction
NH
+HCN HCl N
H
CHO
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H - C N + HCl + -
+ -HC = NH | Cl
NH
H
+ HC = NH | Cl
NH
CH = NHO H2
NH
CHOH2O
H+-NH3
-HCl
Mechanism
a -
b –
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Mannich reaction Indol undergo Mannich reaction with formaldehyde and dimethyl amine to give 3 – dimethylamine indole
O HCl
NH
H
+ H-C- H + HN N
H
CH2 - N
CH3
CH3 H2OCH3
CH3
3 - dimethylamino methylindole
-