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Volume 7
Biosensors Journal
ISSN: 2090-4967
Electrochemistry 2018
June 11-12, 2018
June 11-12, 2018 | Rome, Italy
4
th
International Conference on
Electrochemistry
Electrochemical thiocyanation of aromatic and alkene derivatives
James Y. Becker, Avishai Levy
and
Anna Gitkis
Ben-Gurion University of the Negev, Israel
T
he anodic thiocyanation of aromatic compounds [1, 2] showed both regio- and isomer- selectivity. For example, the para-
thiocyanate isomer was formed exclusively:
SCN- - e → SCN.
2SCN. → (SCN)2
The one-pot anodic thiocyanation and isothiocyanation of alkenes in both acidic two-phase (water-dichloromethane) and
homogeneous one-phase (water-acetonitrile) media will be described too [3, 4]. A selected example of type of products
obtained is illustrated in the scheme below:
becker@bgu.ac.ilBiosens J 2018, Volume 7
DOI: 10.4172/2090-4967-C1-003
OCH
3
OCH
3
SCN
(SCN)
2
+ polymer (SCN)
n
Anode
Me
Me
Me
Me
C C
N
CS
S
CN
Me
Me
Me
Me
C C
S
CN
S
CN
Me
Me
Me
Me
Me
CH
2
OH
Me
Me
C C
OH
S
CN
Me
Me
Me
Me
(1)
(Major)
(2)
(5)
(3)
C C
H
S
CN
Me
Me
Me
Me
(4)
(
trace)
C anode/[SCN]
-
DCM-H
2
O
0.5NH
2
SO
4