3-Hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enone

3-Hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enone

The title compound, C11H16O3, was obtained by reaction of dimedone, 5,5-dimethylcyclohexane-1,3-dione, and α-chloroacetone. The cyclohexenone ring exhibits an envelope conformation with puckering amplitudes Q = 0.433 (2) and Φ = −109.0&#8...

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Bibliographic Details
Main Authors: Jose Camacho, Liz Triana, Simón Hernández-Ortega, Roberto Martínez
Format: Article
Language:English
Published: International Union of Crystallography 2009-12-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536809049046
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spelling doaj-4607101438ed44d08f140027c52918642020-11-24T21:30:36ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682009-12-016512o3186o318610.1107/S16005368090490463-Hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enoneJose CamachoLiz TrianaSimón Hernández-OrtegaRoberto MartínezThe title compound, C11H16O3, was obtained by reaction of dimedone, 5,5-dimethylcyclohexane-1,3-dione, and α-chloroacetone. The cyclohexenone ring exhibits an envelope conformation with puckering amplitudes Q = 0.433 (2) and Φ = −109.0 (3)°. The 2-oxopropyl fragment is almost perpendicular to the cyclohexanone ring [dihedral angle = 77.72 (8)°]. In the crystal, the molecules are linked to each other through O—H...O hydrogen bonding, building a chain parallel to the b axis. http://scripts.iucr.org/cgi-bin/paper?S1600536809049046
collection DOAJ
language English
format Article
sources DOAJ
author Jose Camacho
Liz Triana
Simón Hernández-Ortega
Roberto Martínez
spellingShingle Jose Camacho
Liz Triana
Simón Hernández-Ortega
Roberto Martínez
3-Hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enone
Acta Crystallographica Section E
author_facet Jose Camacho
Liz Triana
Simón Hernández-Ortega
Roberto Martínez
author_sort Jose Camacho
title 3-Hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enone
title_short 3-Hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enone
title_full 3-Hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enone
title_fullStr 3-Hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enone
title_full_unstemmed 3-Hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enone
title_sort 3-hydroxy-5,5-dimethyl-2-(2-oxopropyl)cyclohex-2-enone
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2009-12-01
description The title compound, C11H16O3, was obtained by reaction of dimedone, 5,5-dimethylcyclohexane-1,3-dione, and α-chloroacetone. The cyclohexenone ring exhibits an envelope conformation with puckering amplitudes Q = 0.433 (2) and Φ = −109.0 (3)°. The 2-oxopropyl fragment is almost perpendicular to the cyclohexanone ring [dihedral angle = 77.72 (8)°]. In the crystal, the molecules are linked to each other through O—H...O hydrogen bonding, building a chain parallel to the b axis.
url http://scripts.iucr.org/cgi-bin/paper?S1600536809049046
work_keys_str_mv AT josecamacho 3hydroxy55dimethyl22oxopropylcyclohex2enone
AT liztriana 3hydroxy55dimethyl22oxopropylcyclohex2enone
AT simamp243nhernamp225ndezortega 3hydroxy55dimethyl22oxopropylcyclohex2enone
AT robertomartamp237nez 3hydroxy55dimethyl22oxopropylcyclohex2enone
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