The title compound, C(11)H(14)Cl(2)O, was synthesized by the reaction of a dichloro-methane solution of (R)-carvone and potassium tert-butano-late in the presence of a catalytic amount of benzyl-triethyl-ammonium chloride in chloro-form. The cyclo-hexene ring adopts a half-boat conformation. The cyclo-propyl ring is unsymmetrical, the shortest C-C bond being distal to the alkyl-substituted C atom. The crystal packing is stabilized only by van der Waals inter-actions.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152127PMC
http://dx.doi.org/10.1107/S1600536811021933DOI Listing

Publication Analysis

Top Keywords

5r-5-[1r-22-dichloro-1-methyl-cyclo-prop-yl]-2-methyl-cyclo-hex-2-en-1-one title
4
title compound
4
compound c11h14cl2o
4
c11h14cl2o synthesized
4
synthesized reaction
4
reaction dichloro-methane
4
dichloro-methane solution
4
solution r-carvone
4
r-carvone potassium
4
potassium tert-butano-late
4

Similar Publications

The title compound, C(11)H(14)Cl(2)O, was synthesized by the reaction of a dichloro-methane solution of (R)-carvone and potassium tert-butano-late in the presence of a catalytic amount of benzyl-triethyl-ammonium chloride in chloro-form. The cyclo-hexene ring adopts a half-boat conformation. The cyclo-propyl ring is unsymmetrical, the shortest C-C bond being distal to the alkyl-substituted C atom.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!