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Name Reactions-II PDF
Name Reactions-II PDF
U R
CHEMISTRY BY H. GAUR
GA
ORGANIC CHEMISTRY
H.
BY
NAMED REACTIONS
RY
SHEET-2
IST
E M
ACHARYA INSTITUTE
CH
Contact: +91-8946891920
Visit us: www.hgaurchemistry.com, Email: [email protected]
Contact: +91-8946891920 www.hgaurchemistry.com Page (1)
MANNICH REACTION:
* It Involve the condensation of a compound having active methylene group (active H-atom) with formaldehyde &
H-N< (H–N< NH3 or, NH2R or NHR2 ,but not used NR3) in the presence of acid and formed amino methyl
derivative or substituted amino methyl derivative (Mannich base) is called Mannich Reaction.
| HCl |
G–––C–––H + O + H–N< G–––C––CH2–N<
| || –H2O |
H–C–H Mannich base or
Active H-atom Methanal NH3 or 10-amine Amino Methyl derivative
0
or 2 -amine or
R
0
(But not 3 amine) Substituted amino
methylderivative
U
O O
|| HCl ||
CH3–C–CH2–H + HCHO + R2NH CH3–C–CH2–CH2–NR2
GA
–H2O
Mannich base
Mechanism:
* It is acid catalysed as well as base catalysed.
+
O OH .. R .. R R
|| || R +
_+
H.
R2NH +
CH2–N CH2––N CH2–N
H–C–H + H+ H–C–H CH2–N |
| | R R –H2O R R
OH H OH
+ 2
More Stable
+
BY
O OH O–H
|| || |
H+ CH3–C=CH 2
CH3–C–CH3 CH3–C –CH2–H +
–H
Enol
.. +
OH R OH R O R
| + || || ..
CH3–C=CH2 + CH2 = N CH3–C–CH2–CH2–N CH3–C–CH2–CH2–N
RY
+
R R –H R
Mannich Base
Generally, mannich base, used for the synthesis of , unsaturated carbonyls.
R
IST
.. R–X (1 equ.)
CH3 –C–CH2–CH2 –N CH3–C–CH=CH2
|| R /Ag 2 O ||
O O
Unsaturated carbonyl
M
OH OH
..
H CH2–NR2
CH
+
CH2 = NR2
As a E+
HCl
(2) + HCHO + R2NH
N H N CH2–NR2
| |
H H
O
|| +
H NHR CH2 CH3
H+/HNHR + H
+
R
C––O C O
H H |
|| || H–CH2 H CH3
O O
U
GA
NR O NHR O
In Same H
Manner H–CH2
O
H.
O CH3 O CH3
|| | H+ || |
(4) CH3–C–C–H + HCHO + HNMe2 CH3–C–C–CH2–NMe2
| |
CH3 CH3
BY
Major Product
This H-atom involve in enol formation B’coz of
in acidic medium more substituted enol is the formed.
H CH2–NMe2
(5) HCl
+ HCHO + Me2NH
RY
N N
| |
H H
O O
|| ||
IST
H CH2–NR2
(6) + HCHO + HNR2 HCl
+
M
+ HCHO + R2NH H
(7)
N CH2–H N CH2–CH2–NR2
.. ..
E
H CH2–NR2
OH OH
CH
+
+ HCHO + R2NH H
(9) H CH2–NR2
O O
Acidic H-atom
H –
OH– OH H2 O
+ Intramolecular
Michael O O
O CH3 O addition O CH2 O Aldol Condensation O
–
OH
R
| reaction Enolate ion
H Aldol
–H2O
U
GA
O
Examples of Robinson Annelation Reaction:
Acidic H-atom O
O || CH3
|| H
CH3 (i) OH–
(1)
H.
+
CH3 O (ii) O
O
Acidic H-atom O
O
|| ||
H
BY
(i) OH–
(2) + (ii)
O CH3 O O
Acidic H-atom
COOC2H5
H
COOC2H5
RY
(i) CH3OK/THF
(3) + (ii) K2CO3/MeOH/
CH3 O O
O
* In this reaction, the ester group can be removed by Hydrolysis followed by decarboxylation
COOEt COO–
IST
–
OH / (i)
(ii) H3O+
O O O
O
M
O ||
|| –
Q. CH2O + CH3–C–CH3 OH
? Ans:
(Excess)
E
O OH
||
CH
–
OH | CH2O OH
–
Sol. CH3–C–CH3 CH2=C–CH3 CH2–CH–C–CH3 CH2=CH–C–CH3
| | || –H2O || CH2–C–CH3
Enol OH H O O | ||
H O
O
O O 2||
||6 5 4 3 2 || 1 OH–/ 3 1
CH3–C–CH2 –CH2–CH2 –C–CH2 6
| Intramolecular 4
H Aldol condensation 5 CH3
it is also substrate for
Michael addition
O O O O
|| || || ||
CH–OH
(A) (B) (C) (D) CHO
O
O O
Ans: (B)
R
O O
O O H || ||
|| || H H
H
U
–
C=O OH H2 O
Sol. + CH2–CHO OH–
| –
| O O O OH
O Cl O H
GA
–H2O
O
||
H.
BY
RY
IST
E M
CH
H
BF3/Et2O BuLi BuLi HgCl2
=O A B C D
HS
Q. H
HS Br Br
R
O
S H S S
H Br
U
Ans: H S S S
(A) (B) (C) (D)
GA
SH
R
SH (i) BuLi HgCl2/H2O
=O (A) (B) (C)
Q. H BF3/Et2O O
(ii)
H.
Ph
R S R S R
HO HO
| =O
BY
Ans: H S S Ph
Ph
(A) (B) (C)
SH SH O
H ||
BuLi, Cl–C–OEt H+, HgCl2
C=O (A) (B) (C)
RY
Q. BF3/Et 2O H2O
R
||
CH2–C–OEt R–C–Cl
| +
(ii) H , HgCl2, H2O
Cl
(ii) H+, HgCl2, H2O
(D)
M
(E) (F)
H S R S
E
O O O O O O O
|| || || || || || ||
Ans: S EtO–C S R–C–C–OEt R–C–CH2– R–C–CH2–C–OEt R–C–C–R
R
CH
|| (D) (F)
(A) O (B) (C) (E)
+ –
Li N
R
O O
CH3 || H CH3 ||
LDA –
U
O O
GA
|| – LDA – || –
CH2–C–O CH2–C–O
|
H
– –
COO COO
Ha | Ha | –
CH2–Hb
H.
CH2
LDA
Important Questions:
BY
(i) LDA
(1) R–CH2–C–R ? R–CH–C–R
|| (ii) R–X | ||
O R O
– (i) LDA –
(2) R–CH2–COO ? R–CH–COO
(ii) R1–X |
RY
R1
R1
(i) LDA |
(3) Ph–C–CH–CH=CH2 ? Ph–C–C–CH=CH2
|| | (ii) R1–X || |
IST
O R O R
CH3
(i) LDA
(4) CH3–C–O–CH2–CH3 ? =CH–C–OCH2–CH3
|| (ii) =O CH3 ||
O + O
M
(iii) H3O/
O O
|| || CH3
E
Less Hindard
H CH3
(i) LDA
(6) ?
H (ii) CH3I H
||
O O
D CH3
(i) LDA
(7) ?
H (ii) CH3I H (Acidity of H & D are alsmost same)
C2H5–S
(8) (i) LDA (i) LDA
CH2 ? (A) (B)
(ii) R–C–Cl (ii) CH3
C2H5–S ||
O
||
R
O
U
||
O C2H5–S C–R
C2H5–S ||
GA
CH–C–R C
H.
N
N (i) LDA |
(9) ? Ans: O
| (ii) Ph–C–OEt N ||
N || || C
|| H O Ph
BY
O O O O
|| || || ||
(i) LDA N O
(10) | N O ? Ans:
H (ii) PhCH2I
Ph
RY
H
CH3 |
(11) Br 6 5 | CH2 LDA (i) LDA
2 (A) (B)
3 || 1 (ii) R–C–Cl
4 ||
O
IST
O O
O || ||
R–C
||
CH3
M
CH3
(A) (B)
E
Ph
CH
|
(i) LDA
(12) Ph–C=CH2 ? Ans:
| (i) cis–Ph–CH=CH–Ph
CH3 (iii) HA
Ph Ph
(cis)
Ph
| Ph
C Ph
– |– |
CH2 CH2
HA
H H
C=C Ph Ph Ph Ph
Ph Ph (cis)
cis
This reaction takes place by the concerted mechanism so that symmetry of reactant maintain in the product (i.e., cis cis
& trans trans)
R
Ph
|
U
(i) LDA N–Ar
(13) Ph–C=N–Ar ? Ans:
| (ii) E–Ph–CH=CH–Ph
GA
CH3
(iii) HA Ph Ph
trans
COOEt EtOOC Me
(i) LDA
H.
(14) ? Ans:
(ii) CH3I
t–Bu t–Bu
BY
Solution:
–
O
| EtOOC Me
H C
| – |
OEt OEt OEt
LDA CH3–I
|| ||
O O
RY
t–Bu
R
2. Addition Reaction [AASE]
3. Substitution Reaction
U
4. Elimination Reaction
GA
REFORMATSKY REACTION:
–
OH Zn
H.
Darzen Reaction Reformatsky Reaction
Darzen Reaction:
BY
COOEt
O
–
O OH Major
|| H H
RY
|
+ CH – COOEt O
| ||
Br – CH2–COOEt
OH
Minor
IST
CH2–COOEt + Zn
| Organozinc ester
Br
E
O ZnBr + OH
O H2O/H
|| –
CH
+ CH2–COOEt OH CH2–COOEt
| CH2–COOEt
+ZnBr –Zn
Br -Hydroxy ester
Reactivity w.r.t. Reformatsky reaction.
CH2–COOEt CH2–COOEt CH2–COOEt
Reactivity: | | |
I Br Cl
* RMgX have nucleophilic as well as basic character so it react with acidic-H-atom & give acid-base reaction.
Br–CH2–COOEt
Mg Zn
BrMgCH2–COOEt BrZnCH2–COOEt
Highly reactive Less reactive
R
React with React with ester group reactive carbonyl compound
(Not react with ester)
=O group Mg–CH2– COOEt
U
|
Br
Major Product
GA
Minor Product
(It is side reaction)
H.
OH H
| |
R–C––CH–COOR R2C = CH – COOR
| –H2O
R -Unsaturated ester
* During the reformatsky reaction, zinc enolate formed as a Reformatsky reagent.
BY
O .. O–ZnBr O–Zn–Br O
|| Zn | | ||
Br–CH2–C–OC2H5 CH2=C–OC2 H5 CH2=C–OC2 H5 CH2–C–OC2H5
|
ZnBr
Zinc enolate Organozinc ester
RY
* During the reformatsky reaction, zinc (Zn) behave as two electron dondor
(i) Zn
1. + BrCH2–COOR
CHO (ii) H3O+/ CH=CH–COOR
S S
+
N ZnBr H3 O O
M
|| (H2O/HCl) ||
2. R–C N + BrZnCH2COOR R–C–CH2 –COOR R–C–CH2–COOR + NH4 Cl
OH
–Zn
E
Br
CH3 CH3
CH
| (i) Zn/ether/ |
3. CH3–CHO + Br–C–COOEt CH3–CH–C–COOEt
| (ii) NH4Cl/HOH | |
CH3 OH CH3
CH3
| (i) Zn/C6H6/
4. Ph–CHO + Br–CH–COOEt Ph–CH=C–COOEt
(ii) H2O/H+/ |
CH3
O CH3 OH O CH3
|| (i) Zn/ether/C6H6/ | ||
6. CH3–CH2–CHO + Br–CH2–C–N CH3–CH2–CH–CH2–C–N
CH3 (ii) H2 O/NH4Cl
CH3
–
H2O/ OH/
O CH3
||
R
CH3–CH2–CH=CH–C–N
CH3
U
OH O CH3 – O
| || H2O/ OH/ ||
GA
CH3–CH2–CH–CH2–C–N CH3–CH2–CH=CH–C–N
CH3
H.
BY
RY
IST
E M
CH
R
Dry Ether
R–X + Mg RMgX
Grignard reagent
U
Mechanism:
GA
+ –
R–X R + X
R+ + Mg R– + Mg
+2
– +2 –
R + Mg + X RMgX
* Etheral solution of Grignard Reagent is used for the synthetic application because of it is highly reactive.
H.
R
O
R R
BY
Mg
R X
O
R
* Solvated form of RMgX is stable. It can not be isolate in individual form (i.e., pure form)
RY
R––X RMgX
Hard
C–Na
C–Li
Above this hard
CH
C–Mg
C–Al Below this soft
C–Zn
C–Pb
C–Cd * Ionic bond in C-Na & C-Li
C–Sn * In all other, polar covalent bond
C–Cu
C–Hg
Soft
R––X
R––X
R–X
R––I > R–Br > R–Cl 1 > 20 > 30
0
X
X X
Due to leaving group ability of halide
> >
R
Due to stability of carbonion (RMgX)
U
Points about the preparation of Grignard Reagent:
GA
1. Compounds having acidic H-atom can not be used in preparation of Grignard Reagent.
Mg/Dry Ether
C––C––C––C No Grignard Reagent
| |
G X
G = Functional groups having active H-atom like: –NH2, –OH,–SH, –COOH etc.
H.
2. 1,2-dihaloalkanes (Vicinal) are not used for the preparation of Grignard Reagent.
Mg/Ether
C––C No Grignard Reagent but formed C = C + Mg X2
| |
BY
X X
Mg/Ether
3. C––C No Grignard Reagent but formed C = C
| |
X L
RY
CH2–X
5. 1,4- & higher dihalides may be used for the preparation of Grignard Reagent
X
|
M
6. m- & p- may be used for the preparation of Grignard Reagent but O-form is not used because of,
X
E
X
Mg/ Ether (Et2O)
CH
X
o-Dihalo benzene Benzyne Dimer
7. Generally allylic & benzylic halides are not used for the preparation of Grignard Reagent. (Also rarely used so
answer give according to option)
8. .. Mg/ Et2O
CH2=CH–Cl No Grignard reagent
In the reaction Grignard reagent is not formed, because of, during the reaction high temperature is required which
is greater than boiling point of Et2O but if THF is used then.
CH2=CH–Br
Mg/THF
CH2=CH–MgBr
R
Cl
U
|
GA
Br
Mg(1equ.)/ Mg(excess)/
Mg(excess)/ THF
1 equ. Mg/ Et2O THF
Et2O
MgCl
H.
Cl Cl
| | |
Cl
|
Bronstate basicity
:Lewis Besicity
Acid-Base Reaction:
M
Z
– +
R Mg X + H–––Z R–H + Mg
CH
X
High Electronegative atom. Like
O, N, F, S or sp-hybrid-carbon
Above reaction takes place in
Due to Aramaticity
RMgX
R
H––C C–CH 2–CH 2–O H Two equ. RMgX is used.
* The reactivity of the compounds w.r.t. RMgX would be high which have more acidic H-atom, so that
U
Acidity of H-atom ses reactivity w.r.t. Grignard reagent ses
GA
* During the acid base reaction Grignard reagent behave as the Bronstate base.
H.
Alcohols
BY
0
0 2 -Alcohol 0
1 -Alcohol O2 3 -Alcohol
From O2 O2
O
O || O
|| R–C–H ||
H–C–H R–C–R
O
O || O
RY
H–C–Z ||
R–C–Z
Oxirane (Except-Amide)
(Except-Amide)
Reaction with O2 :
IST
H3O+
RMgX + ½O2 RO Mg X R–OH
0 0 0 0 0 0
1,2,3 1 , 2 , 3 -Alcohol
Nature of Alcohol is depends on the Alkyl groups in grignard reagent
M
R in G.R. R–OH
If then
E
0
Me–, 1 , 2 , 3
0 0
MeOH, , 10, 20, 30 -Alcohol
CH
0
H–CHO 1–Alcohol
* Formation of MeOH is not possible
R–CHO 0
2– Alcohol
0
R–C=O 3– Alcohol
|
R
R
– +
O – O Mg X O
|| + | ||
R Mg X
U
Y–C–L Y–C–L Y–C–R
| X
R –Mg Carbonyl compounds
L
GA
H or R
*
Acid halide,
Ester or Anhydride
* MeOH & 10 alcohol can not be formed by this reaction
– +
Y O Mg X
H.
O OH
|| RMgX H3 O
+ |
0
Y–C–R Y–C–R If Y = H = 2 alcohol
R R X | 0
–Mg R Y = R = 3 alcohol
BY
L
O
|| R OMgX
O R R
OMgX
RY
RMgX R
O + RMg X O
OMgX
|| OMgX
O O O ||
Succinic anthydride O
IST
+
H2O/H
R OH
R
M
OH
||
E
O
CH
O R OH
||
(i) RMgX R
O + ? Ans. OH
(ii) H2O/H
|| ||
O O
Phthalic anhydride
R
R R
If Grignard reagent react with the unsmmetrical epoxide ring, then ring opening takes place from the less hindrad
U
site.
O – Mg +X OH
O H3O
+
GA
– +
R Mg X +
R R R R R
* Here: o-atom can be replaced by the other hetero atom like S, N etc.
* Prepared alcohol have two C-atom more than the R of Grignard reagent
But in case of carbonyl only one C-atom more than the R of G.R.
H.
if the case of
(i) O2 with RMgX = ROH of same C
(ii) =O with RMgX = ROH of more than one C.
BY
(iii)
O with RMgX = ROH of more than two C.
(i) RMgX
Q. R–C C–H
O
? R–C C–CH2–CH–OH
RY
|
(ii) R
R
(iii) H2O
D
IST
Q. Br MgBr
1 equ. Mg D2 O
(A) (B) Ans.
Et2O OD Cl
Cl Cl
–Mg (A) (B)
Br
M
* Preparation of Acid:
+
H3O
RMgX + O = C = O R–C–OMgX R–C–OH
E
|| ||
O O
CH
* Preparation of Cyanide:
C N CH3–C=NMgX O
||
N.A.R H 3O+ CH3 Because of RMgX finish
+ CH3MgX
(Excess) due to acidification
Acetophenone
* If is best method for preparation of acetophenone
CN O CH3 OH
||
Q.
(i) CH3MgX (i) CH3 MgBr CH3 CH3
+ (A) + (B) Ans.
(ii) H2O/H (ii) H2 O/H
R
(A) (B)
CN
U
CH3 OH
(i) CH3MgX
Q. ? CH3
GA
+
(ii) H2O/H
(iii) CH3MgBr
+
(iv) H2O/H
RMgX
Assuming both condition as excess
* or
H.
RMgX(excess)
* Reaction with ketene:
+
H3O
CH2=C=O + CH3MgBr CH2=C–O–Mg+Br CH2=C–O–H CH2–C=O
BY
| | | |
CH3 CH3 H CH3
H3O+
R–CH = C = O + R–Mg+X R–CH–C=O
+
| |
E H R
Nu– Nu–
E+
RY
.. +
OEt OEt OEt OEt
RMgBr/MgBr2 + RMgX
H––C––OEt H––C––OEt H––C H––C
IST
+ OEt
OEt OEt OEt OEt
–Mg
Ortho ester Br
MgBr
M
OEt OH O
H2O/H
+
||
H––C H––C R–C–H
| | –H2O
E
R OEt R OH
CH
OEt
H––C––OEt + RMgX R – CHO
|
R OEt
R
Cyclohexane
U
Solution:
GA
– +
O Mg Br OH
CH3MgBr CH3MgBr H2O/O+
CH2=C=O + Br2 CH2–C=O CH2–C=O CH2––C CH––C
| | | | | | CH3 | | CH
Br Br Br CH3 Br CH3 Br CH3 3
(B)
(A)
H.
O CH3
(C)
CH3
BY
* Reaction With Alkylhalide:
MgBr
O
Q. + ?
MgBr
M
Solution:
BrMg
E
O BrMg O
|| O– Mg+Br OH
C + H3O+
CH
6-membered cyclic
* Allylic Grignard reagent react with the allylic shift.
O
|| RMgX
No reaction
* If the Grignard reagent has H-atom then following reaction takes place.
R
O O– Mg+Br OH OH
|| H2O/H+
+ CH2–CH2–MgBr + Mg
| –CH2=CH2 Br
U
H H
GA
G.R. & Michael Addition:
Michael addition takes plcae only in acyclic , unsaturated ketones with G.R. (in carbonyl compounds)
RMgX
O or Ar Michael
||
C6H5–CH=CH–C–CH3
H.
Unsaturated Ketone RLi
Direct
But in
O RMgX
Direct
BY
RLi
Direct
Unsaturated
cyclic ketone
RY
RMgX
O Direct
||
C6H5–CH=CH–C–H
Unsaturated RLi
Direct
aldehyde
IST
O R OH
||
R
Q. O (i) RMgX(excess)
+ ? Ans. OH
(ii) H2O/H
M
OH
(i) RMgX(excess) OH
Q. R–CH ? |
E
+
(ii) H 2O/H Ans. R–CH–R
OEt
CH
O
|| O
Q. RMgX + Cl–C–OEt ? ||
(1equ.) Ans. R–C–OEt
O OH
|| + |
H2O/H
Q. RMgX + Cl–C–OEt ? Ans. R––C––R
|
(excess) R
R
Excess Ethyl carbonate OH
30- Alcohol
U
* Best Grignard reagent CH3MgI
* In Grignard reagent R Alkyl group, phenyl group, allylic group but not vinyl group.
GA
* Solvated form of RMgX is stable. It can not be isolated in individual (pure) form.
R
R O
R
Mg
H.
R X
O
Solvated form
R
* Solvents for RMgX Saturated ethers
BY
O
O O
THF 1,4-dioxane
RY
Similarly:
– +
M
O O OH O O Mg X O
|| || | || RMgX | ||
CH3–C–CH2–C–CH3 CH3–C=CH–C–CH3 CH3––C=CH–––C–CH3 + R – H
Acetylacetone
E
H2O/H+
RMgX + S RS– Mg+X R–SH
X
Thiols
–Mg
OH
Cl
RMgX + Cl–NH2 R–NH2 + Mg
Amine X
R’–MgX + R–O–CH2X R–O–CH2R’ + MgX2
Ether
Contact: +91-8946891920 www.hgaurchemistry.com Page (22)
CH3
|
CH3–C–MgX
O |
|| (i) CH3
Q. CH –CH–C–CH ? No Reaction Due to Steric hindrance
3 3
| (ii) H2O/H
+
CH3
U R
GA
H.
BY
RY
IST
E M
CH
H3 O+
RLi + O = C = O R–C=O R–C=O
Excess | |
OLi OH
Carboxylic acid
R
* When RLi in excess:
U
R R O
– + RLi | H3O
+ | ||
– +
RLi + O = C = O R–C–O Li R–C–O Li R–C–OH R–C–R
|| |– + | –H2O
GA
Excess O Ketone
O Li OH
* Reaction with Carboxylic Acid:
O O O– Li+
|| || RLi | H3O+
R–C–OH + RLi R–C–O– Li+ R–C–O– Li+ R–C–R
| ||
H.
R O
Symmetric ketone
* Similarly:
BY
O O
|| (i) RLi ||
––––C–OH +
––––C–R
(ii) H2O/H
With reaction in configuration
O
||
RY
O O
OH R H
H+ BuLi – Li+
+ O=C –H2O –BuH
R R O
OH O
E M
–+
+ R–C–OLi
||
CH
O
Cyclo hexene
* RLi has advantage over Grignard reaction when the Grignard reaction is fail to react with highly hindard carbonyl
group, the oganolithium react with such compound to give normal product.
O OH
|| –––Li |
–––C––– +
–––C–––
(ii) H2O/H |
Tritertiary butyl-carbinol
Na/Liq.NH3 – +
R–C C–H R–C C Na
–
Work as a Nu
D2O R’–X
R
(D)
U
Solution:
Na/Liq.NH3
GA
+ – – +
H–C C–H Na C C Na (A)
R–X D2O
R–C C–R D–C C–D
(B) (D)
Na/liq. NH3
H.
(Birch reduction)
R H
C=C
BY
H (C) R
Trans-Alkene
Lithation Reaction:
* It is addition of Lithium
RY
+ BuLi + BuH
*
N CH2–H N CH2 –Li+
IST
F F
H Li
* + BuLi
M
Behave as Nu–
BuLi & give substitution reaction
E
* Li
O O
CH
Behave as Nu–
BuLi
*
N N Li
* For Pyridine, first preority lithation (acid-base reaction) after then chichibabine reaction (second priority)
BuLi
O O Li
OMe OMe
BuLi
*
Br Li
R
* R C C H BuLi
R C C Li
U
* CH 2 C CH 2 BuLi
CH 2 C CHLi
* CH 2 CH CH 3 BuLi
CH 2 CH CH 2 Li
GA
*S + BuLi
S S S
Li
H.
BY
RY
IST
E M
CH
R
RMgX |
R–C–OH 30-Alcohol
O H2O/H+ |
|| R
R–C–Cl
O
+I –I R2Cd || R2Cd
R–C–R No reaction
(Dialkyl cadmium) +I +I
R
RMgX > R2Cd
O Rosenmund O
U
|| catalyst ||
R–C–Cl R–C–H
or
GA
* DIBAL
or
t-Bu3SnH
H.
O
||
(CH3)2Cd CH3
O (A)
|| (Small)
COOH
BY
O CH3 CH3
* || (CH3)2Cd
O O (B)
(Excess)
||
O
RY
R2CuLi
R
CH3 CH3
Cu
U
Li Li
Cu CH3
GA
CH3
H.
* It is very weak base so in the presence of Gilmann reagent present, halides does not give elimination reactions.
* It is replacement method of the wurtz reaction.
Dry ether
R–X + 2Na + X–R R––R
BY
Wurtz reaction
Higher alkanes
R2CuLi + R’–X R–R’
Corey-House
Reaction Higher alkane
* & by using this method we can also prepared alkanes having odd number of C-atom (corey-house method)
RY
Reagents:
R2CuLi or
RMgX / CuCl
or
IST
CuI
or
RLi / CuCl or CuI
or
R/Cu
M
R
Allylic, Proparglylic,
Benzylic
U
1
* R–C–Cl + R 2CuLi R–C–R 1
|| ||
O O
GA
* In the case of Allylic & propargyl substrates, allylic shift will be takes place (Migration of n-bond or SN 2 ' mechanism)
always.
* Epoxides ring opening takes place from less hindard side (if possible alylic shift or SN 2 ' - mechanism takes place.)
H.
Nu–
O
* Epoxide ring opening take place always anti periplaner manner.
R 2CuLi
Q.1 CH3–(CH2)4 –CH2 –I ? Ans. CH3(CH 2)4CH2–R
BY
X R
| |
R2CuLi
Q.2 ? Ans.
R 2CuLi
Q.3 CH2=CH–X Ans. CH2=CH–R
RY
?
R2CuLi R–C–R
Q.4 R–C–Cl ? Ans. ||
|| O
O
Br
IST
H CH3
+ ? H CH3
C=C
Q.5 CH CuLi Ans. C=C
3 CH3
2 CH3
CH3
M
R R
(CH3)2CuLi
Q.6 Ans. | CH3
CH
?
O OH
O=C–R
COCl
R2CuLi
Q.7 ? Ans.
NO2
NO2
R2CuLi
?
Q.9 OAC Ans.
R
R2CuLi
Q.10 CH3O–C–CH2–CH2–C–Cl ? Ans. CH3O–C–CH2–CH2–C–R
|| || || ||
O O O O
R
(CH3)2CuLi
? OH
U
Q.11 H2O/H+ Ans.
O
CH3 5 6
GA
5 6 CH31 4
7
C=O
7
(CH3)2CuLi
4 ? 2 3 OH
3 O
Q.12 2 O Ans. or
CH3–CH2–CH=CH–CH2 –CH2–COOH
Hept- 4- enoic acid
H.
Michael Addition:
–
O O O–H O
H
H2 O
+ (CH3)2 CuLi CH3 CH3 CH3
BY
CH3
CH3 CH3 CH3
O
||
CH3 –C–Cl
O
COCH3
RY
CH3
CH3
CH3
IST
(CH3)2CuLi
Q.1 + ? Ans.
H2O/H
O O
M
O
||
E
R
CH
? ? ? ?
O OH OH O
|| R R R
R
R
R R R
Via michael R
Via direct Via direct Via michael
addition addition addition addition
COOEt
O COOEt COOEt
||
(CH3)2 CuLi R–C–Cl CH3
Q.4 (A) (B) Ans.
O Et2O
– CH3
O O
COR
(A) (B)
R
Cyclisation Reaction:
–
O O O
U
|| ||
(CH3)2CuLi
GA
Br Br
CH3 CH3
Questions:
H CH3
H Br
(CH 3)2CuLi C=C
Q.1 C=C ? Ans. Et
H.
H
Et H E-Alkene
H H H
(CH3) 2CuLi H
Q.2 C=C ? Ans. C=C
Ph
BY
Br Ph CH3
Z-Alkene
(CH3)2CuLi
?
Q.3 Via SN2 Ans. CH3
RY
OTs Mechanism
Inversion in configuration
O O
|| (CH 3) 2CuLi ||
Q.4 Ph–C–CH2–CH2–OTs ? Ans. Ph–C–CH2–CH2–CH3
IST
CH3 CH3
| (CH3)2CuLi |
Q.5 CH2=C–CH
|
–CH3
Via SN2
? Ans. CH3–CH2–C=CH–CH3
OCOCH3 Mechanism
M
CH3 CH3
O
|| (CH3)2 CuLi
E
CH3
| CH3
(CH3)2CuLi
Q.7 CH C–C–OCOCH3 2 ? Ans. CH3–CH=C=C
| Via SN CH3
CH3 Mechanism
CH3
(i) (CH3 )2CuLi
Q.8 O + ? Ans. + Enantiomer
(ii) H2O/H
2 OH
* SN Mechanism
C CH
(i) (CH3)2CuLi C=CH–CH3
O ?
Q.10 Via SN2 Ans.
Mechanism OH
* Michael addition takes place at less substituted C–C double bond.
* In biocylic , unsaturated ketones always only cis product will be formed.
* In chiral centre containing , unsaturated ketones, give two diastereomeric product.
R
O O CH3
|| CH3 (i) (CH3)2CuLi ||
U
Q.1 Ph–CH=CH–C–CH=C ? Ans. Ph–CH–CH
|
2 –C–CH=C
GA
O O
O
|| ||
||
(i) (CH3)2CuLi +
+
? CH3 CH3
Q.2 (ii) H2O/H Ans. 10%
*| CH3 90% CH3
H.
CH3
Trans + enantiomer Cis + Enantiomer
CH3 CH3
(i) (CH3)2CuLi
BY
Q.3 O ? Ans. O
(ii) H2O/H+ 100%
CH3
cis-product
RY
IST
E M
CH