Journal of Organic Chemistry 2004-02-20

Accelerated Koenigs-Knorr glucuronidation of a deactivated nitrophenol: unveiling the role of polyamine additive 1,1,4,7,10,10-hexamethyltriethylenetetramine through design of experiments.

Federica Stazi, Giovanni Palmisano, Marco Turconi, Simona Clini, Marco Santagostino

Index: J. Org. Chem. 69(4) , 1097-103, (2004)

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Abstract

1,1,4,7,10,10-Hexamethyltriethylenetetramine (HMTTA) emerged from a limited parallel screening of selected polyamines as the most appropriate additive for an especially problematic Koenigs-Knorr glucuronidation. This initial finding rapidly evolved into a reliable and high-yielding procedure through the use of two sets of experimental designs. The detailed effect of the stoichiometry of reagents and the amount of amine additive on reaction yield was elucidated. The complexity of the response surface for product yield, described by a third-order polynomial equation, together with ancillary kinetic experiments evidenced the multiple role of HMTTA in the present glucuronidation process.

Related Compounds

  • Disilver(1+) carbo...
  • 1,1,4,7,10,10-Hexa...

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