Akta Kimia Indonesia
Vol 5, No 1 (2020)

Synthesis of the BCAC4ND2 Ionophore from p-t-Butylcalix[4]arene Ethylester

Nasriadi Dali Wela (Jurusan Kimia FMIPA UHO Kendari)
Arniah Dali Wela (Jurusan Pendidikan Kimia FMIPA UHO Kendari)



Article Info

Publish Date
06 Apr 2020

Abstract

Abstrak Penelitian tentang sintesis ionofor BCAC4ND2 dari p-t-butilkaliks[4]arena etilester telah dilakukan. Penelitian ini bertujuan untuk mensintesis ionofor BCAC4ND2 dari p-t-butilkaliks[4]arena etilester. Ionofor BCAC4ND2 disintesis dengan cara menghidrolisis p-t-butilkaliks[4]arena etilester dalam larutan KOH-etanol 95%. Reaksi hidrolisis ester terpromosi basa ini direfluks selama 28 jam pada suhu 78 oC. Ionofor BCAC4ND2 diidentifikasi dan dikarakterisasi dengan titik leleh, kromatografi lapis tipis (KLT), spektrometer FTIR, 1H-NMR, dan 13C-NMR. Ionofor BCAC4ND2 yang diperoleh berupa padatan putih (perolehan 62,38%), titik leleh 326-328 oC, dan KLT (SiO2, etanol : etilasetat = 1 : 1 v/v, Rf = 0,93).Abstract Research on the synthesis of the BCAC4ND2 ionophore from p-t-butylcalix[4]arene ethylester has been carried out. This study aims to synthesize the BCAC4ND2 ionophor from p-t-butylcalix[4]arene ethylester. The BCAC4ND2 ionophore is synthesized by hydrolyzing p-t-butylcalix[4]arene ethylester in aqueous KOH-ethanol of 95%. The hydrolysis reaction of these base-promoted esters are refluxed for 28 hours at 78 oC. The BCAC4ND2 ionophore was identified and characterized by melting point, thin layer chromatography (TLC), FTIR, 1H-NMR, and 13C-NMR spectrometers. The BCAC4ND2 ionophore obtained was in the form of white solid (62.38% recovery), a melting point 326-328 oC, and TLC (SiO2, ethanol : ethylacetate = 1 : 1 v/v, Rf = 0.93).

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Journal Info

Abbrev

kimia

Publisher

Subject

Chemistry

Description

Akta Kimia Indoneisa publishes peer-reviewed open access articles in all areas of chemistry, including: Analytical Chemistry Physical Chemistry Organic Chemistry Inorganic Chemistry Biological Chemistry To submit an article, you need to register first. Please click register in ...