Di-tert-Butyl 2,2′-[2,2′-methyl­enebis(naphthalene-2,1-diyldi­oxy)]diacetate

In the title compound, C(33)H(36)O(6), two naphthalene ring systems are connected through a methyl­ene linkage [C—C—C = 114.9 (2)°]; the ring systems are aligned at an angle of 76.5 (1)°. Of the two –O–CH(2)–C(=O)–C(CH(3))(3) substituents, one adopts an extended conformation whereas the other is U-s...

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Detalles Bibliográficos
Autores principales: Ali, Qamar, Anis, Itrat, Raza Shah, M., Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051626/
https://www.ncbi.nlm.nih.gov/pubmed/21523181
http://dx.doi.org/10.1107/S1600536811003291
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author Ali, Qamar
Anis, Itrat
Raza Shah, M.
Ng, Seik Weng
author_facet Ali, Qamar
Anis, Itrat
Raza Shah, M.
Ng, Seik Weng
author_sort Ali, Qamar
collection PubMed
description In the title compound, C(33)H(36)O(6), two naphthalene ring systems are connected through a methyl­ene linkage [C—C—C = 114.9 (2)°]; the ring systems are aligned at an angle of 76.5 (1)°. Of the two –O–CH(2)–C(=O)–C(CH(3))(3) substituents, one adopts an extended conformation whereas the other is U-shaped. In the crystal, mol­ecules are linked via weak C—H⋯O hydrogen bonding, forming supra­molecular chains running along the c axis.
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spelling pubmed-30516262011-04-26 Di-tert-Butyl 2,2′-[2,2′-methyl­enebis(naphthalene-2,1-diyldi­oxy)]diacetate Ali, Qamar Anis, Itrat Raza Shah, M. Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(33)H(36)O(6), two naphthalene ring systems are connected through a methyl­ene linkage [C—C—C = 114.9 (2)°]; the ring systems are aligned at an angle of 76.5 (1)°. Of the two –O–CH(2)–C(=O)–C(CH(3))(3) substituents, one adopts an extended conformation whereas the other is U-shaped. In the crystal, mol­ecules are linked via weak C—H⋯O hydrogen bonding, forming supra­molecular chains running along the c axis. International Union of Crystallography 2011-01-29 /pmc/articles/PMC3051626/ /pubmed/21523181 http://dx.doi.org/10.1107/S1600536811003291 Text en © Ali et al. 2011 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
Ali, Qamar
Anis, Itrat
Raza Shah, M.
Ng, Seik Weng
Di-tert-Butyl 2,2′-[2,2′-methyl­enebis(naphthalene-2,1-diyldi­oxy)]diacetate
title Di-tert-Butyl 2,2′-[2,2′-methyl­enebis(naphthalene-2,1-diyldi­oxy)]diacetate
title_full Di-tert-Butyl 2,2′-[2,2′-methyl­enebis(naphthalene-2,1-diyldi­oxy)]diacetate
title_fullStr Di-tert-Butyl 2,2′-[2,2′-methyl­enebis(naphthalene-2,1-diyldi­oxy)]diacetate
title_full_unstemmed Di-tert-Butyl 2,2′-[2,2′-methyl­enebis(naphthalene-2,1-diyldi­oxy)]diacetate
title_short Di-tert-Butyl 2,2′-[2,2′-methyl­enebis(naphthalene-2,1-diyldi­oxy)]diacetate
title_sort di-tert-butyl 2,2′-[2,2′-methyl­enebis(naphthalene-2,1-diyldi­oxy)]diacetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051626/
https://www.ncbi.nlm.nih.gov/pubmed/21523181
http://dx.doi.org/10.1107/S1600536811003291
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AT anisitrat ditertbutyl2222methylenebisnaphthalene21diyldioxydiacetate
AT razashahm ditertbutyl2222methylenebisnaphthalene21diyldioxydiacetate
AT ngseikweng ditertbutyl2222methylenebisnaphthalene21diyldioxydiacetate

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