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Formation of Tertiary 3-Nitro Allylic Alcohol by Condensation of 2-Chloroiso- butyrophenone with Nitromethanide Anion: Estimation of Gibbs Free Enthalpies of Reaction in Solution for the Reaction Mechanism [1]

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Summary.

The reaction of 2-chloroisobutyrophenones and nitromethanide anion gives stereoselectively (E)-3-nitro allylic alcohols. The Gibbs free enthalpies of reaction in DMSO for carbanion addition, epoxide formation, and rearrangement to 3-nitro allylic alcohol, as elementary steps for the reaction, were estimated from corresponding neutral gas reactions and using a thermodynamical approach to the transfer of gaseous compounds to DMSO. A criterion for assigning the sign of affinity of liquid compounds to DMSO was developed on the basis of the Gibbs enthalpies of liquefaction. The information obtained on reaction rate and thermodynamic viability of the steps indicates that carbanion addition is the rate-determining step.

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Authors and Affiliations

  1. Instituto de Química Médica, CSIC, E-28006, Madrid, Spain

    Francisco Ros & Inmaculada Barbero

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  1. Francisco Ros
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  2. Inmaculada Barbero
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Correspondence to Francisco Ros.

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In memory of Prof. Dr. M. Ballester, deceased on April 6, 2005

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Ros, F., Barbero, I. Formation of Tertiary 3-Nitro Allylic Alcohol by Condensation of 2-Chloroiso- butyrophenone with Nitromethanide Anion: Estimation of Gibbs Free Enthalpies of Reaction in Solution for the Reaction Mechanism [1]. Monatsh. Chem. 136, 1607–1617 (2005). https://doi.org/10.1007/s00706-005-0340-9

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  • DOI: https://doi.org/10.1007/s00706-005-0340-9

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