Molecules (Feb 1998)

An Improved Synthesis of Homocitrate

  • Ji-Qing Xu,
  • Zeng-Chun Li

DOI
https://doi.org/10.3390/30200031
Journal volume & issue
Vol. 3, no. 2
pp. 31 – 34

Abstract

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Monoethyl malonate (1) and tert-butyl alcohol are esterified by catalysis with dicyclohexylcarbodiimide and 4-dimethylaminopyridine to yield ethyl t-butyl malonate (2). The ethoxymagnesio derivative (3) of the ester is condensed with b-carbomethoxypropionyl chloride to give the triester (4), which is decomposed by heating under vacuum in the presence of b-naphthalensulfonic acid to give ethyl methyl β-ketoadipate (5). Compound 5 is reacted with hydrogen cyanide,followed by hydrolysis of the cyanohydrin to give the free acid (6). Compound 6 is converted to homocitrate (7) by the use of an improved procedure.

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