Carbonyl Chemistry IIwillson.cm.utexas.edu/Teaching/Ch391/Files/CH391lecture8.pdfChemistry 391...
Transcript of Carbonyl Chemistry IIwillson.cm.utexas.edu/Teaching/Ch391/Files/CH391lecture8.pdfChemistry 391...
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Carbonyl Chemistry IICarbonyl Chemistry II
++CCOO--
CCOO
Lecture 8Lecture 8Chemistry 391 10/20/02
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Chemistry 391 10/23/02
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Reaction ThemeReaction ThemeThe most common reaction of a carbonyl group is addition of a nucleophile to form a tetrahedral addition compound
Tetrahedral carbonyl addition compound
+ CR
RO CNu
O -
RR
Nu -
Here it is an acid or electrophile
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Chemistry 391 10/23/02
Carbon Carbon NucleophilesNucleophilesAddition of carbon nucleophiles is one of the most important types of nucleophilic additions to a C=O group; a new carbona new carbon--carbon bondcarbon bond is formed in the process!!!!
We will study the addition of these carbonnucleophiles
A Grignard reagent
An organolithium reagent
An anion of a terminal alkyne
Cyanide ion
RC C - NRMgX RLi - C
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Chemistry 391 10/23/02
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Chemistry 391 10/23/02
See Ashby, E.C., Smith , M.B. J. Chem Soc. 1964, 86 4363 and references thereto…I consider the detailed structure of this reagent to still be a topic of research!
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Chemistry 391 10/23/02
GrignardGrignard ReactionsReactions
Mg+2H3O+
CH3CH2- MgBr+
HC
HO CH3CH2 C
H
H
O- MgBr+CH3CH2 C
H
H
OH +THF dil.
Mg+2H3O+
CH3CH2- MgBr+ C
HO CH3CH2 C
H
O- MgBr+ +THF dil.
CH3CH2 C
H
OH
Mg+2H3O+
CH3CH2- MgBr+ CH3CH2 C O- MgBr+
CH3
CH2
CH2
CH3
+THF dil.
CH3CH2 C OH
CH3
CH2
CH2
CH3
C O
CH3
CH2
CH2
CH3
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Chemistry 391 10/23/02
Grignard Reactions
Mg+2H3O+
CH3CH2- MgBr+ CH3CH2 C O- MgBr+
O
+THF dil.
CH3CH2 C OH
O
C OO
MgBrO
THFO-MgBr+
H3O+
Dilute
OH
These are valuable and important reactions…
Please add to your card stock!
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GrignardGrignard reagents react with estersreagents react with esters
––++
RR CC
OO••••
•••• ••••
OCHOCH33••••••••
R'R'
RR
MgXMgX
CC
OO
••••••••
δδ–– δδ++ OCHOCH33••••••••
R'R' diethyldiethyletherether
MgXMgX
but species formed is but species formed is unstable and dissociates unstable and dissociates under the reaction under the reaction conditions to form a ketoneconditions to form a ketone
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GrignardGrignard reagents react with estersreagents react with esters
––++
RR CC
OO••••
•••• ••••
diethyldiethyletherether OCHOCH33
••••••••
R'R'
––CHCH33OOMgXMgX
RR
MgXMgX
CC
OO
••••••••
δδ–– δδ++ OCHOCH33••••••••
R'R'
MgXMgX
this ketone then goes this ketone then goes on to react with a on to react with a second mole of thesecond mole of theGrignardGrignard reagent to reagent to give a tertiary alcohol
CC
OO
RR R'R'
••••••••give a tertiary alcohol
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ExampleExample
2 CH2 CH33MgBrMgBr ++ (CH(CH33))22CHCCHCOCHOCH33
OO
1. diethyl ether1. diethyl ether
2. H2. H33OO++
Two of the groups Two of the groups attached to the attached to the tertiary carbon tertiary carbon come from thecome from theGrignardGrignard reagent
(CH(CH33))22CHCCHCCHCH33
OHOH
CHCH33reagent
(73%)(73%)
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Chemistry 391 10/23/02
Sorry, but This Does NOT work!!!!
But……
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Chemistry 391 10/23/02
This does!!
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Chemistry 391 10/23/02
HH22CC CHLiCHLi CHCH
OOOrganolithiumOrganolithium ReagentsReagents
++
1. diethyl ether1. diethyl ether
2. H2. H33OO++
CHCH22CHCHCHCH
OHOH(76%)(76%)
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Chemistry 391 10/23/02
Salts of Terminal AlkynesSalts of Terminal AlkynesAddition of an acetylide anion followed by H3O+ gives an α-acetylenic alcohol
Mg+2H3O++
THF dil.C O
CH3
CH2
CH2
CH3
C O- MgBr+
CH3
CH2
CH2
CH3
C OH
CH3
CH2
CH2
CH3
RC C- Na+ RC C RC C
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Chemistry 391 10/23/02
Salts of Terminal Salts of Terminal AlkynesAlkynes
HO C
OCCH3HO
HO CH2 CH
O
H2 SO 4 , HgSO4
H2 O
2 . H 2O2 , NaOH
An α-hydroxyketone
α
β
α
CH
1 B2H6
A β-hydroxyaldehyde
Write the mechanism using the arrow convention
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Chemistry 391 10/23/02
O
HC C1) Na, THF
2) H3O+
CHC
OH1) B2H6, THF
2) H2O2, NaOH
HO CH2CH
O
O
HC C1) Na, THF
2) H3O+
CHC
OH ?????
HO
O
CH3
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Chemistry 391 10/23/02
MECHANISM FOR REACTION OF MECHANISM FOR REACTION OF ALKENES WITH BHALKENES WITH BH33
Step 1:A concerted reaction. The π electrons act as thenucleophile with the electrophilic B and the H is transferred to the C with syn stereochemistry.
Step 2:First step repeats twice more so that all of the B-H bonds react with C=C to produce the trialkylborane
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Chemistry 391 10/23/02
Step 3:Peroxide ion reacts as the nucleophile with theelectrophilic B atom.
Step 4:Migration of C-B bond to form a C-O bond and displace hydroxide. Stereochemistry of C center is retained.
Step 5:Attack of hydroxide as a nucleophile with theelectrophilic B displacing the alkoxide.
Step 6:An acid / base reaction to form the alcohol.
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Chemistry 391 10/23/02
Another variant on the Another variant on the WittigWittig reaction that is much easier and reaction that is much easier and cheaper to carry out is called thecheaper to carry out is called the WittigWittig--Horner reactionHorner reaction. This . This uses auses a phosphitephosphite ester instead of aester instead of a phosphinephosphine::
E/Z is an interesting issue and still not fully clear.Triphenylphosphines tend normally to give the Z- (or cis-) isomer. Trialkylphosphines or the presence of groups thatstabilise the ylide tend to give E- (or trans-) geometry. So take your pick!
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Chemistry 391 10/23/02
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Chemistry 391 10/23/02
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Chemistry 391 10/23/02
Addition of HCNAddition of HCNMechanism of cyanohydrin formation
N C- H3O+
THF dil.C O
CH3
CH2
CH2
CH3
C O-
CH3
CH2
CH2
CH3
N C Mg+2+C OH
CH3
CH2
CH2
CH3
N C
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Chemistry 391 10/23/02
CyanohydrinsCyanohydrinsThe value of cyanohydrins is for the new functional groups into which they can be converted– acid-catalyzed dehydration of the 2° alcohol gives a
valuable monomer
Propenenitrile (Acrylonitrile)
+
acid catalyst
2-Hydroxypropanenitrile (Acetaldehyde cyanohydrin)
CH3 CHC N
OH
NCH2 =CHC H2 O
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Chemistry 391 10/23/02
CyanohydrinsCyanohydrins– acid-catalyzed hydrolysis of the cyano group
gives an α-hydroxycarboxylic acid
acid catalyst
Benzaldehyde cyanohydrin (Mandelonitrile)
2-Hydroxy-2-phenyl- ethanoic acid
(Mandelic acid)
+N
OH
CHC CHCOH
HO OH2 O
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Chemistry 391 10/23/02
CyanohydrinsCyanohydrins– catalytic reduction of the carbon-nitrogen
triple bond converts the cyano group gives a 1° amine
Benzaldehyde cyanohydrin 2-Amino-1-phenylethanol
Ni+CHC
OH
NOH
CHCH2 NH22 H2
LiAlH4 also works well...LiAlH4 also works well...
But…what about Pd/C and H2But…what about Pd/C and H2
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Chemistry 391 10/23/02
WittigWittig ReactionReactionThe Wittig reaction is a very versatile synthetic method for the synthesis of alkenes fromaldehydes and ketones.
Triphenyl- phosphine oxide
Methylene- cyclohexane
A phosphonium ylide
+
+-+
+
O
CH2 Ph 3 P-O -
Ph 3 P-CH 2
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Chemistry 391 10/23/02
Phosphonium YlidesPhosphonium YlidesYlideYlide: a molecule which, when written in a Lewis structure showing all atoms with complete valence shells, has positive and negative charges on adjacent atoms
Phosphonium ylidesPhosphonium ylides are formed in two steps: 1. treatment of triphenylphosphine with a 1° or 2°
alkyl halide to form a phosphonium salt followed by 2. treatment of the phosphonium salt with strong base,
typically butyllithium
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Chemistry 391 10/23/02
Phosphonium YlidesPhosphonium Ylides
An alkyltriphenyl-phosphonium iodide
+Ph 3 P-CH 3 I-S N2
Triphenyl-phosphine
+Ph 3 P CH3 -I
+CH3 CH2 CH2 CH2 Li + + H-CH 2 -PPh 3 I -
Butyllithium
•• +-CH2 -PPh 3 + + Li + I -CH3 CH2 CH2 CH3
A phosphonium ylide
Butane
Ph3P+ CH2-
Ph3P CH2
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Chemistry 391 10/23/02
WittigWittig ReactionReactionPhosphonium ylides react with the C=O group of aldehydes or ketones to give alkenes
Triphenylphosphine oxide
An alkene
+
-••+
An oxaphosphetane
•••• •• ••
-
+•• ••
••
CH2
CR2 O
CH2
CR2
CH2
CR2O
Ph 3 P Ph 3 P
O
Ph 3 P
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Chemistry 391 10/23/02
WittigWittig ReactionReactionexamples
-++
+ 1-Phenyl-2-butene (87% Z isomer; 13% E isomer)
+
O
PhCH 2 CH Ph 3 P-CHCH 3
PhCH 2 CH=CHCH 3 Ph 3 P-O -
What about the E/Z ratio…??What about the E/Z ratio…??
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Chemistry 391 10/23/02
WittigWittig ReactionReactionExamples:
++ -
+2-Methyl-2-heptene
+
O
CH3
CH3 CCH3 Ph 3 P-CH(CH 2 ) 3 CH3
CH3 C=CH(CH2 ) 3 CH3 Ph 3 P-O -
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Chemistry 391 10/23/02
A variant on the Wittig reaction that is much easier and cheaper to carry out is called the Wittig-Horner reaction. This uses a phosphite ester instead of a phosphine:
The Wittig-Horner reaction
The ylide is much more reactive in this case.
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Chemistry 391 10/23/02
TheThe WittigWittig ReactionReaction“ Cis/trans, E/Z etc. Well, that's an interesting issue though still not fully clear.Triphenylphosphines tend normally to give the Z- (or cis-) isomer. Trialkylphosphines or the presence of groups that stabilise the ylide tends to give E- (or trans-) geometry. So take your pick! What makes the Wittig reaction so useful is that it can tolerate all kinds of functionality”.
http://www.sunderland.ac.uk/~hs0bcl/org8.htm
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Chemistry 391 10/23/02
++ -
+
Ethyl (E)-4-phenyl-2-butenoate (only the E isomer is formed)
+
O O
Ph 3 P-O -
PhCH 2 CH Ph 3 P-CHCOCH 2 CH3
H
C CCOCH2 CH3
PhCH 2 H
O
So….this is not so easy!!
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Chemistry 391 10/23/02
Homework: Due Wed 10/29Homework: Due Wed 10/29
Read Chapter 15 and “learn” the reactions on pages 752 –754
Do: 15.27, 15.33, 15.35a,b, 15.39, 15.41, 15.45 and the 10 synthesis problems on the web page!