Section 16.10 Synthesis of Substituted Benzenes Using Arenediazonium Salts 647
KCl and KBr cannot be used in place of CuCl and CuBr in Sandmeyer reactions; the
cuprous salts are required. This indicates that the cuprous ion is involved in the reac-
tion, most likely by serving as a radical initiator (Section 4.10).
Although chloro and bromo substituents can be placed directly on a benzene ring
by halogenation, the Sandmeyer reaction can be a useful alternative. For example, if
you wanted to make para-chloroethylbenzene, chlorination of ethylbenzene would
lead to a mixture of the ortho and para isomers.
However, if you started with para-ethylaniline and used a Sandmeyer reaction for
chlorination, only the desired para product would be formed.
PROBLEM 20
Explain why a diazonium group on a benzene ring cannot be used to direct an incoming
substituent to the meta position.
p-ethylaniline p-chloroethylbenzene
NaNO 2 , HCl
0 °C
CH 2 CH 3
NH 2
CuCl
CH 2 CH 3 CH 2 CH 3
N+ NCl− Cl
FeCl 3
CH 2 CH 3
++Cl 2
CH 2 CH 3
Cl
CH 2 CH 3
ethylbenzene o-chloroethylbenzene Cl
p-chloroethylbenzene
CuC
N
+
NCl−
Br
CN
+ N 2
Br
N
m-bromobenzenediazonium chloride m-bromobenzonitrile
CuBr
NNBr−
+
Br
+ N 2
CuCl
NNCl−
+
Cl
CH 3 CH 3
+ N 2
Sandmeyer reactions
benzenediazonium
bromide
bromobenzene
p-toluenediazonium
chloride
p-chlorotoluene
Traugott Sandmeyer (1854–1922)
was born in Switzerland. He received
a Ph.D. from the University of
Heidelberg and discovered the
reaction that bears his name in 1884.
He was a scientist at Geigy Co. in
Basel, Switzerland.