Cargando…

Practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles

(1,1,2,2-Tetrafluorobut-3-en-1-yl)zinc bromide was prepared by insertion of the zinc–silver couple into the CF(2)–Br bond of commercially available 4-bromo-3,3,4,4-tetrafluorobut-1-ene in DMF at 0 °C for 0.5 h, The resultant polyfluorinated zinc reagent was found to be thermally stable at ambient te...

Descripción completa

Detalles Bibliográficos
Autores principales: Tamamoto, Ken, Yamada, Shigeyuki, Konno, Tsutomu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142754/
https://www.ncbi.nlm.nih.gov/pubmed/30254702
http://dx.doi.org/10.3762/bjoc.14.213
_version_ 1783355889762172928
author Tamamoto, Ken
Yamada, Shigeyuki
Konno, Tsutomu
author_facet Tamamoto, Ken
Yamada, Shigeyuki
Konno, Tsutomu
author_sort Tamamoto, Ken
collection PubMed
description (1,1,2,2-Tetrafluorobut-3-en-1-yl)zinc bromide was prepared by insertion of the zinc–silver couple into the CF(2)–Br bond of commercially available 4-bromo-3,3,4,4-tetrafluorobut-1-ene in DMF at 0 °C for 0.5 h, The resultant polyfluorinated zinc reagent was found to be thermally stable at ambient temperature and storable for at least 1.5 years in the refrigerator. This CF(2)CF(2)-containing organozinc reagent could be easily transmetallated to copper species, which underwent cross-coupling reactions with various aromatic iodides or acyl chlorides to produce a broad range of CF(2)CF(2)-containing organic molecules in good-to-excellent yields. Therefore, the zinc reagent could become a new and practical synthetic tool for producing functional molecules with a CF(2)CF(2) fragment.
format Online
Article
Text
id pubmed-6142754
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-61427542018-09-25 Practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles Tamamoto, Ken Yamada, Shigeyuki Konno, Tsutomu Beilstein J Org Chem Full Research Paper (1,1,2,2-Tetrafluorobut-3-en-1-yl)zinc bromide was prepared by insertion of the zinc–silver couple into the CF(2)–Br bond of commercially available 4-bromo-3,3,4,4-tetrafluorobut-1-ene in DMF at 0 °C for 0.5 h, The resultant polyfluorinated zinc reagent was found to be thermally stable at ambient temperature and storable for at least 1.5 years in the refrigerator. This CF(2)CF(2)-containing organozinc reagent could be easily transmetallated to copper species, which underwent cross-coupling reactions with various aromatic iodides or acyl chlorides to produce a broad range of CF(2)CF(2)-containing organic molecules in good-to-excellent yields. Therefore, the zinc reagent could become a new and practical synthetic tool for producing functional molecules with a CF(2)CF(2) fragment. Beilstein-Institut 2018-09-11 /pmc/articles/PMC6142754/ /pubmed/30254702 http://dx.doi.org/10.3762/bjoc.14.213 Text en Copyright © 2018, Tamamoto et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Tamamoto, Ken
Yamada, Shigeyuki
Konno, Tsutomu
Practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles
title Practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles
title_full Practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles
title_fullStr Practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles
title_full_unstemmed Practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles
title_short Practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles
title_sort practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142754/
https://www.ncbi.nlm.nih.gov/pubmed/30254702
http://dx.doi.org/10.3762/bjoc.14.213
work_keys_str_mv AT tamamotoken practicaltetrafluoroethylenefragmentinstallationthroughacouplingreactionof1122tetrafluorobut3en1ylzincbromidewithvariouselectrophiles
AT yamadashigeyuki practicaltetrafluoroethylenefragmentinstallationthroughacouplingreactionof1122tetrafluorobut3en1ylzincbromidewithvariouselectrophiles
AT konnotsutomu practicaltetrafluoroethylenefragmentinstallationthroughacouplingreactionof1122tetrafluorobut3en1ylzincbromidewithvariouselectrophiles