Pharmaciana (Nov 2014)

SINTESIS SENYAWA N-(2-NITROBENZIL)-1,10 FENANTROLINIUM KLORIDA DARI 2-NITROBENZIL KLORIDA DAN 1,10-FENANTROLIN MONOHIDRAT

  • Artie Noor Pratiwi,
  • Nurkhasanah Mahfudh

DOI
https://doi.org/10.12928/pharmaciana.v4i2.1563
Journal volume & issue
Vol. 4, no. 2
pp. 93 – 100

Abstract

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The compound N-(2-nitrobenzyl)-1,10-phenantrolinium chloride has been synthesized by nucleophilic substitution reaction bimolecular (SN2) between the 2-nitrobenzyl chloride with 1,10-fenantrolin monohydrate. This study is an experimental research of Organic Synthesis. Synthesis is done by varying the compound 2-nitrobenzyl chloride to 1.10 Phenantroline monohydrate ie 1:1, 3:1, 5:1 and 7:1. The purity of the compounds synthesized are determined based on the melting range data and TLC. Identification of the structure of the compounds synthesized done by spectrometry UV/Visible, IR and GC-MS. The results of this research is a colorless amorphous solid from N-(2-nitrobenzyl)-1,10-phenantrolinium chloride with an optimal yield 37%+5% and the variation of mole 2-nitrobenzyl chloride effect on the amount of yield product, there is an optimal yield in the mole ratio of 1:1.

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