(3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate

The title compound, C20H18O6, prepared from d-mannitol by a two-step procedure, is a functionalized fused bis-tetrahydrofuran. In the central fragment, consisting of two fused tetrahydrofuran rings, one O atom and its two adjacent C atoms, a methylene and a bridgehead C atom, are disordered over two...

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Main Authors: Vincenzo Piccialli, Sabrina Zaccaria, Nicola Borbone, Roberto Centore, Angela Tuzi
Format: Article
Language:English
Published: International Union of Crystallography 2013-09-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536813021612
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spelling doaj-184cc7e25fb4470597db64c5006840302020-11-24T21:28:00ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682013-09-01699o1396o139710.1107/S1600536813021612(3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoateVincenzo PiccialliSabrina ZaccariaNicola BorboneRoberto CentoreAngela TuziThe title compound, C20H18O6, prepared from d-mannitol by a two-step procedure, is a functionalized fused bis-tetrahydrofuran. In the central fragment, consisting of two fused tetrahydrofuran rings, one O atom and its two adjacent C atoms, a methylene and a bridgehead C atom, are disordered over two sets of sites with an occupancy ratio of 0.735 (9):0.265 (9). In the major component, the ring containing the disordered O atom is a half-chair conformation with twisted methylene and benzoate-substituted C atoms, whereas the other ring has a half-chair or T-form conformation. In the minor component, the ring with the disordered O atom has an envelope conformation, with the O atom as the flap, and the other ring has a half-chair conformation, with the O atom and the other bridgehead CH atom being twisted. The two aromatic rings are inclined to one another by 20.00 (12)°. In the crystal, adjacent molecules are linked via C—H...π interactions, forming chains propagating along [010].http://scripts.iucr.org/cgi-bin/paper?S1600536813021612
collection DOAJ
language English
format Article
sources DOAJ
author Vincenzo Piccialli
Sabrina Zaccaria
Nicola Borbone
Roberto Centore
Angela Tuzi
spellingShingle Vincenzo Piccialli
Sabrina Zaccaria
Nicola Borbone
Roberto Centore
Angela Tuzi
(3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate
Acta Crystallographica Section E
author_facet Vincenzo Piccialli
Sabrina Zaccaria
Nicola Borbone
Roberto Centore
Angela Tuzi
author_sort Vincenzo Piccialli
title (3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate
title_short (3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate
title_full (3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate
title_fullStr (3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate
title_full_unstemmed (3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate
title_sort (3r,3ar,6r,6ar)-hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2013-09-01
description The title compound, C20H18O6, prepared from d-mannitol by a two-step procedure, is a functionalized fused bis-tetrahydrofuran. In the central fragment, consisting of two fused tetrahydrofuran rings, one O atom and its two adjacent C atoms, a methylene and a bridgehead C atom, are disordered over two sets of sites with an occupancy ratio of 0.735 (9):0.265 (9). In the major component, the ring containing the disordered O atom is a half-chair conformation with twisted methylene and benzoate-substituted C atoms, whereas the other ring has a half-chair or T-form conformation. In the minor component, the ring with the disordered O atom has an envelope conformation, with the O atom as the flap, and the other ring has a half-chair conformation, with the O atom and the other bridgehead CH atom being twisted. The two aromatic rings are inclined to one another by 20.00 (12)°. In the crystal, adjacent molecules are linked via C—H...π interactions, forming chains propagating along [010].
url http://scripts.iucr.org/cgi-bin/paper?S1600536813021612
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