Chem 634 Spring 2015
Nucleophilic Substitution Chemistry
Announcements
Organic Journal Club: Thursdays, 12:30–1:30, 219 BRL
Contact: Corey Basch (cbasch@udel.edu) organizes the OJC website and schedule.
Today
a) alcohol activation
b) substitutions at alkyl centers
c) ester formation
d) amide formation
Reading: C&S 3.1-3.2, 3.4
Alkyl Nucleophilic Substitution
Be sure you understand SN1, SN2 and elimination mechanisms.
Common Problem:
OH
Me
Me
Nuc
Nuc
Nuc
Me
Me
OH
(poor leaving group)
Need to activate ROH
Sulfonates
O
O
OH
Me
O
S
Cl
O
R
Me
Me
"py"
N
py
Me
O O
Cl
H O S
R
Me
O
S
Me
R
note retention
Sulfonates
common sulfonates
O
S
O
O
S Me
O
O
S CF3
O
Me
toluenesulfonate
"tosylate" "Ts"
common reagents
O
Cl S
O
Me
(TsCl)
methanesulfonate
"mesylate" "Ms"
trifluoromethanesulfonate
"trifate" "Tf"
MsCl
O
O
F3C S O S CF3
O
O
(Tf2O)
Note: alkyl triflates are normally unstable
Sulfonates
Recall:
R1
R1
Nuc
LG
Nuc
R2
H
R1
LG
Nuc
H
R2
R2 H
σ*C-LG
transition state
OSO2Me
Me
Me
Nuc
Nuc
SN2
Me
Me
LG
Sulfonates
O
O
S
OH
Me
O
Cl
O
R
Me
Me
O
S
Me
R
retention
"py"
N
OSO2Me
Me
Me
Nuc
SN2
Me
Nuc
overall inversion!
Me
inversion
Alkyl Halides
Formation of alkyl chlorides:
OH
Me
Cl
Me
O
S
Cl
Cl
CH2Cl2, py
O
Me
O
S
Cl
Me
Cl
pyH+
thionyl chloride
Me
Me
+ SO2, pyHCl
Alkyl Halides
Cl
Me
Nuc
Nuc
Me
Me
Me
note: overall rentention
compared to R–OH
Alkyl Halides
Formation of alkyl bromides:
PPh3, Br2
R
OH
R
Br
Alkyl Halides
Formation of alkyl bromides:
Mechanism:
Ph3P
Br Br
Ph3P Br
Br
ROH
Br
R
H
O
R
PPh3
O
- HBr
PPh3
- Ph3P O
Br
Ph3P O
Ph3P O
triphenylphosphine oxide
very thermodynamically favorable
R
Br
Alkyl Halides
Similar reactions for ROH to RX:
X = Br
X = Cl
PBr3
PCl3
O
PPh3 + CCl4
PPh3
+
N Br
N-Bromosuccinimide
"NBS"
O
X=I
PPh3
+
I2
+ imidazole
N
N
H
You need to be able to draw the mechanisms for these reactions.
The Finkelstein Reaction
R
Br
+
NaI
R
I
+
NaBr
not soluble
in acetone
Pg 170 in Kurti & Czako
Reactivity of Alkyl Electrophiles
For RX
TfO>>>>>TsO > I > MsO > Br >> Cl
unstable
sluggish
Most Often Used RX in SN2-type Reactions
Br
Me-I
benzyl bromide
"BnBr"
Cl
allyl chloride
WHY?
Small or activated.
No beta-hydrogen atoms.
NO E2!
Nuc
H
Me
Me
X
How to Control SN2 vs E2
Me
H
Me
X
Nuc
vs
Me
Nuc
SN2
E2
small nucleophiles
“non-basic” nucleophiles
methyl, 1° or 2° substrates
large nucleophiles
“basic” nucleophiles
3° substrates (SN2 very rare)
Note: In most cases, SN2 vs E2 compete.
“Basic” vs “Non-Basic”
MUST KNOW pKa TABLE
(every organic
chemist should know
these)
Note water and
DMSO numbers do
not match. Why?
For SN2 vs E2, cutoff is ~ pKa = 12-16
Also see: Evans pKa Table (Harvard)
Reich pKa Table (UW Madison) http://www2.lsdiv.harvard.edu/labs/evans/pdf/evans_pKa_table.pdf
http://www.chem.wisc.edu/areas/reich/pkatable/index.htm
Using pKa to Predict Equilibrium
Consider:
Treat As:
MeOLi + Bu-H
MeOH + BuLi
MeOH + Bu-
Karxn =?
MeO- + Bu-H
Ignores counter-ion. Not a prefect assumption. In some cases, down right bad, but it gives us a start.
Definitions:
BuH + H2O
MeO-
MeOH + H2O
Ka2
Ka1 = 10-50
Bu- + H3O+
=
+ H3
[MeO-][H3O+]
[MeOH][H2O]
O+
pka1 = 50
Ka2 = 10-17
pka2 = 17
=10-17
Using pKa to Predict Equilibrium
Bu- + H3O+
BuH + H2O
BuH + H2O
rewrite: Bu- + H3O+
Ka3
=
[BuH][H2O]
[Bu-][H3O+]
Ka3 = 1/Ka1 =1/10-50
=1/10-50
Using pKa to Predict Equilibrium
MeOH + Bu-
[MeO-][BuH]
Karxn =
=
MeO- + Bu-H
[Bu-][MeOH]
[MeO-][H3O+]
[MeOH][H2O]
·
= Ka2 • Ka3
[BuH][H2O]
[Bu-][H3O+]
= 10-17 • 1/10-50
= 10(-17-(-50)) = 1033
Note: pKa(Bu–H) = 50
pKa(MeO–H) = 17
Alkylation With Carbon Nucleophiles
R
CN
Br
Na+,
–CN
K+
R
CN
pKa 9.4 (12.9)
Note: C–C bond formed
We will see many more carbon nucleophiles later in the class.
Oxygen Nucleophiles
"Williamson Ether Synthesis"
R
OH
pKa (30)
MeI, NaH
pKa' ~36
R
OMe
For 1° & 2° RX, E2 can compete
OH
Ph
Br
O
K2CO3
pKa 10 (18)
O
Typically solvent is DMF or DMSO
H
NMe2
Me
O
S
Me
Oxygen Nucleophiles
O
R
O
BnBr
OH
Cs2CO3
DMF
R
OBn
Mitsunobu Reaction
DEAD
Me
Me
OH
Me
Me
PPh3, RCO2H
R
O
O
O
DEAD =
EtO
O
N N
OEt
Upsides:
•  works with many acidic nucleophiles
•  clean SN2 chemistry
•  often works when other reactions won't
Downsides:
•  DEAD not overly stable
•  waste
Mitsunobu, Synthesis, 1981,1, 1
Mitsunobu Reaction
Mechanism:
O
O
O
O
N N
EtO
OEt
EtO
N N
PPh3
O
O
PPh3
O
EtO
O
N N
H
PPh3
N N
H
EtO
OEt
O
R
OEt
OEt
PPh3
H O
OH
R'
H
O
R"
R'
R"
O
O
EtO
O
N N
H H
waste
OEt
R'
R
O
O PPh3
+
O
R"
O
R'
R
R"
+ OPPh3
waste
Nitrogen Nucleophiles
Challenge: Overalkylation…
NH2
Me–I
N
H
Me
+
Me
N
Me
+
Me
Me
N
Me
I
Nitrogen Nucleophiles
Classical: Gabriel Synthesis
O
NK
O
+
R
R
Br
+ KBr
N
O
O
O
H2N NH2
R
NH2
+
2 steps
HN
HN
O
Nitrogen Nucleophiles
Azides
Me
Me
Br
NaN3
pKa' 7.9
Me
Me
[Red]
Me
N3
Caution!:
•  NaN3 ~1000x more toxic than NaCN
•  Azides can explode
Me
NH2
Nitrogen Nucleophiles
Amides
soft
O
R
O
MeI
NHEt
Cs2CO3
DMF
O
MeO S OMe
O
dimethyl sulfate
LiAlH4
N Et
Me
R
hard
OMe
R
NMe
"imidate"
R
N Et
Me