SYNTHESIS OF ANALOG L--METIL-DOPA FROM EUGENOL

https://doi.org/10.22146/ijc.21788

Hanoch J Sohilait(1*), Hardjono Sastrohamidjojo(2), Sabirin Matsjeh(3), J Stuart Grossert(4)

(1) epartment of Chemistry, Faculty of Mathematics and Natural Sciences Pattimura University, Kampus PGSD, Ambon
(2) Department of Chemistry, Faculty of Mathematics and Natural Sciences Gadjah Mada University, Sekip Utara Yogyakarta
(3) Department of Chemistry, Faculty of Mathematics and Natural Sciences Gadjah Mada University, Sekip Utara Yogyakarta
(4) epartment of Chemistry, Dalhousie University Nova Scotia, Canada
(*) Corresponding Author

Abstract


Synthesis of analog L--metil-Dopa from eugenol has been achieved through conversion of allyl group to ketone, followed by reaction with NH3 and KCN and by hydrolisis. The addition reaction of methyleugenol with formic acid yield methyleugenyl formate (60,69%). The hydrolis of methyileugenylformate with KOH in aqaueous-ethanolic solution produced methyleugenyl alcohol (73,68%). The oxidation of methyleugenyl alcohol with PCC yield methyleugenyl ketone (67,71%). The reaction of methyleugenyl ketone with NH3 and KCN yield D,L--amino--(3,4-dimetoxybenzyl) propionitril (84,14%). The hydrolisis of D,L--amino--(3,4-dimetoxybenzyl) propionitril with concentrated hydrochloric acid gave Analog L--metil-Dopa as a main target (91,98%). The structure elucidation of these products were analyzed by FTIR, 1H-NMR, 13C-NMR and MS

 

Keywords: Analog L--metil-Dopa; eugenol.


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DOI: https://doi.org/10.22146/ijc.21788

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Indonesian Journal of Chemisty (ISSN 1411-9420 / 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

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