ISSN : 0970 - 020X, ONLINE ISSN : 2231-5039
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Abstract

A Novel Synthetic Route to Perkin's Dye and Acid - Assisted Nucleophilic Rupture of C-N-P Linkages by Kinetic Means

L. N. Gupta, R. Singh and Shashi Prabha


Abstract:

The extreme stability of o-nitro-p-anisidine phosphoric diamide allowed its study to be conducted in 40% propionic acid-water system at 98°C ± 0.5°C. The various kinetic variables employed lead to the contribution of monoprotonated form only between 0.1-4.0 M-HCI, alongwith a constant contribution of the zwitterionic form (or the neutral species) in the entire (0.1-7.0 M, HCL) acid range examined. The optimum reactivity at 0.5 M HCL favours weakly basic character of the diamidate, due to abnormal short range interactions of the o-nitro-group with the reaction site. Bimolecular elimination with P-N cleavage is strengthened by various concepts and Arrhenius parameters etc. The diamidate was synthesized from phosphorous pentachloride rather than by POCL3, the latter resulting in the formation of the famous Perkin's dye.

Keywords:

anisidine; zwitterionic; anisidine pentachloride

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