Nucleophilic Aryloxydefluorination of Pentafluorobenzene Without Noble Metal Catalysis | Sciact - CRIS-system of Boreskov Institute of Catalysis

Nucleophilic Aryloxydefluorination of Pentafluorobenzene Without Noble Metal Catalysis Full article

Journal

Journal of Fluorine Chemistry
ISSN: 0022-1139

Output data

Year: 2013, Volume: 153, Pages: 165-167 Pages count : 3 DOI: 10.1016/j.jfluchem.2013.05.016

Tags

NMR spectroscopy, Nucleophilic substitution, Pentafluorobenzene, Phenol

Authors

Adonin Nicolay Yu. ¹ , Bardin Vadim V. ²

Affiliations

1	G.K. Boreskov Institute of Catalysis, SB RAS, Acad. Lavrentjev Ave. 5, 630090 Novosibirsk, Russian Federation
2	N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, SB RAS, Acad. Lavrentjev Ave. 9, 630090 Novosibirsk, Russian Federation

1-Phenoxy-2,3,5,6-tetrafluorobenzene and 1-(4′-fluorophenoxy)-2,3,5,6-tetrafluorobenzene were prepared in a quantitative yield from C6F5H, ArOH and K2CO3 (DMF or DMSO, 120 °C, 9–11 h). The catalytic effect of Pd(OAc)2 in the presence of AgNO3 as claimed in Ref. [1] was not confirmed.

Adonin N.Y. , Bardin V.V.
Nucleophilic Aryloxydefluorination of Pentafluorobenzene Without Noble Metal Catalysis
Journal of Fluorine Chemistry. 2013. V.153. P.165-167. DOI: 10.1016/j.jfluchem.2013.05.016 WOS Scopus РИНЦ ANCAN OpenAlex

Submitted:	Apr 8, 2013
Accepted:	May 15, 2013
Published online:	May 31, 2013
Published print:	Sep 1, 2013

Web of science:	WOS:000322940700024
Scopus:	2-s2.0-84884902342
Elibrary:	21878608
Chemical Abstracts:	2013:1002370
Chemical Abstracts (print):	159:275140
OpenAlex:	W2949975443

DB	Citing
Web of science	9
Scopus	9
Elibrary	8
OpenAlex	10