TY - JOUR
T1 - Silica gel-assisted preparation of 2,4,7-trihalobenzo[b]thiophenes and 4,7-dihalobenzo[b]thiophenes
AU - Mikami, Shinichi
AU - Tanaka, Hiroki
AU - Kishi, Hiroki
AU - Yoshida, Shuhei
AU - Toyota, Kozo
N1 - Publisher Copyright:
© 2019, © 2019 Taylor & Francis Group, LLC.
PY - 2019/7/3
Y1 - 2019/7/3
N2 - All 6 isomers of (bromo)(chloro)(iodo)benzo[b]thiophenes containing three different halogen atoms at the 2-, 4- and 7-positions were synthesized from the corresponding 2-(1-adamantylsulfanyl)-1,4-dihalo-3-(haloethynyl)benzene derivatives, through treatment with silica gel under thermal conditions. In contrast to our previous method using gold chloride catalyst, migration of adamantyl group did not occur in this method using silica gel. Moreover, by using this method, we synthesized 6 types of 4,7-dihalobenzo[b]thiophenes in 4 steps from 2-fluoro-3,6-dihalo-benzaldehydes in moderate to excellent overall yields, 42–82%.
AB - All 6 isomers of (bromo)(chloro)(iodo)benzo[b]thiophenes containing three different halogen atoms at the 2-, 4- and 7-positions were synthesized from the corresponding 2-(1-adamantylsulfanyl)-1,4-dihalo-3-(haloethynyl)benzene derivatives, through treatment with silica gel under thermal conditions. In contrast to our previous method using gold chloride catalyst, migration of adamantyl group did not occur in this method using silica gel. Moreover, by using this method, we synthesized 6 types of 4,7-dihalobenzo[b]thiophenes in 4 steps from 2-fluoro-3,6-dihalo-benzaldehydes in moderate to excellent overall yields, 42–82%.
KW - facile cyclization
KW - fused thiophene
KW - heterocycle
KW - Multihalo-benzo[b]thiophene
KW - quasi T-shape molecular scaffold
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U2 - 10.1080/10426507.2019.1603725
DO - 10.1080/10426507.2019.1603725
M3 - Article
AN - SCOPUS:85064682976
SN - 1042-6507
VL - 194
SP - 768
EP - 770
JO - Phosphorus, Sulfur and Silicon and the Related Elements
JF - Phosphorus, Sulfur and Silicon and the Related Elements
IS - 7
ER -