Now continue on to Problem 14.
PROBLEM 14
How could each of the following compounds be prepared from a ketone and an alkyl
halide?
19.9 Alkylation and Acylation of the -Carbon via
an Enamine Intermediate
We have seen that an enamine is formed when an aldehyde or a ketone reacts with a
secondary amine (Section 18.6).
Enamines react with electrophiles in the same way that enolates do.
N
E+
N+
enamine enolate
O−
E+
O
EE
O
++H 2 O
N
H
N
enamine
catalytic
H+
pyrrolidine
secondary amine
A
O
CH 2 CHCCH 2 CH 3
CH 3
O
a. CH 3 CCH 2 CH 2 CH CH 2 b.
802 CHAPTER 19 Carbonyl Compounds III
CH 3 CH 2 CCH 2 CH 3
O
3-pentanone
CH 3 CH 2 CCH 2 CH 2 CH 3
O
CH 3 CH 2 CCHCH 3
O
CH 3 CH 2 CCHCH 2 CH 3
O
3-hexanone
LDA CH 3 CH 2 Br
LDA
CH 3 Br CH 3 Br
− CH^3 CH^2 CCHCH^3
O
− CH^3 CHCCH^2 CH^2 CH^3
O
+ −
CH 3 CH 2 CCHCH 2 CH 3
O
CH 3 CHCCH 2 CH 2 CH 3
O
+
CH 2 CH 3
4-methyl-3-hexanone
CH 3
4-methyl-3-hexanone
CH 3
2-methyl-3-hexanone