(1-Bromo­naphthalen-2-yl)acetonitrile

The title compound, C(12)H(8)BrN, was prepared as a starting material for a Suzuki cross-coupling reaction with a pinacol ester. The torsion angle about the ring–methylene C—C bond is 30.7 (3)°, such that the N atom is displaced by 1.174 (4) Å from the plane of the naphthalene ring system....

Descripción completa

Detalles Bibliográficos
Autores principales: Harris, Andria D., Baucom, Amy D., Brown, Jessica L., Jones, Daniel S., Ogle, Craig A.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961673/
https://www.ncbi.nlm.nih.gov/pubmed/21202915
http://dx.doi.org/10.1107/S1600536808017418
_version_ 1782189038679097344
author Harris, Andria D.
Baucom, Amy D.
Brown, Jessica L.
Jones, Daniel S.
Ogle, Craig A.
author_facet Harris, Andria D.
Baucom, Amy D.
Brown, Jessica L.
Jones, Daniel S.
Ogle, Craig A.
author_sort Harris, Andria D.
collection PubMed
description The title compound, C(12)H(8)BrN, was prepared as a starting material for a Suzuki cross-coupling reaction with a pinacol ester. The torsion angle about the ring–methylene C—C bond is 30.7 (3)°, such that the N atom is displaced by 1.174 (4) Å from the plane of the naphthalene ring system.
format Text
id pubmed-2961673
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29616732010-12-30 (1-Bromo­naphthalen-2-yl)acetonitrile Harris, Andria D. Baucom, Amy D. Brown, Jessica L. Jones, Daniel S. Ogle, Craig A. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(8)BrN, was prepared as a starting material for a Suzuki cross-coupling reaction with a pinacol ester. The torsion angle about the ring–methylene C—C bond is 30.7 (3)°, such that the N atom is displaced by 1.174 (4) Å from the plane of the naphthalene ring system. International Union of Crystallography 2008-06-19 /pmc/articles/PMC2961673/ /pubmed/21202915 http://dx.doi.org/10.1107/S1600536808017418 Text en © Harris et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Harris, Andria D.
Baucom, Amy D.
Brown, Jessica L.
Jones, Daniel S.
Ogle, Craig A.
(1-Bromo­naphthalen-2-yl)acetonitrile
title (1-Bromo­naphthalen-2-yl)acetonitrile
title_full (1-Bromo­naphthalen-2-yl)acetonitrile
title_fullStr (1-Bromo­naphthalen-2-yl)acetonitrile
title_full_unstemmed (1-Bromo­naphthalen-2-yl)acetonitrile
title_short (1-Bromo­naphthalen-2-yl)acetonitrile
title_sort (1-bromo­naphthalen-2-yl)acetonitrile
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961673/
https://www.ncbi.nlm.nih.gov/pubmed/21202915
http://dx.doi.org/10.1107/S1600536808017418
work_keys_str_mv AT harrisandriad 1bromonaphthalen2ylacetonitrile
AT baucomamyd 1bromonaphthalen2ylacetonitrile
AT brownjessical 1bromonaphthalen2ylacetonitrile
AT jonesdaniels 1bromonaphthalen2ylacetonitrile
AT oglecraiga 1bromonaphthalen2ylacetonitrile

Ejemplares similares