THE SYNTHESIS OF IMIDAZOLIUM-BASED IONIC LIQUID AND ITS APPLICATION IN THE SYNTHESIS OF 2-OXAZOLIDINONE COMPOUNDS USING MAOS (MICROWAVE-ASSISTED ORGANIC SYNTHESIS) METHOD
Carbon dioxide is one of the environmental pollution sources. Through research, it has been discovered that carbon dioxide is a readily available and harmless source of C? atoms. Carbon dioxide has a significant role in the synthesis of 2 oxazolidinone compounds. Conventional methods for produc...
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Format: | Final Project |
Language: | Indonesia |
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Online Access: | https://digilib.itb.ac.id/gdl/view/80708 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Carbon dioxide is one of the environmental pollution sources. Through
research, it has been discovered that carbon dioxide is a readily available and harmless
source of C? atoms. Carbon dioxide has a significant role in the synthesis of 2
oxazolidinone compounds. Conventional methods for producing this compound
involve the use of harmful and toxic chemicals, but a solution can be found by utilizing
carbon dioxide in an ionic liquid medium. The ionic liquid used is 1,3-dimethyl-2,4,5
triphenylimidazolium iodide ([DMTPI]I). The synthesis of ionic liquid ([DMTPI]I)
and 2-oxazolidinone was conducted using the MAOS (Microwave-Assisted Organic
Synthesis) method. The benzoin compound was oxidized with the assistance of copper
(II) acetate, resulting in the formation of 1,2-diphenylethane-1,2-diones or benzyl
compounds. The synthesis of benzyl was conducted using the MAOS method (100
watts) was carried out at 60 ? for 60 minutes resulting in a yield of 60.8%. Then the
benzyl compound was used as a precursor to synthesize 2,4,5-triphenylimidazole or
lophine compounds. Synthesis of lophine compounds by MAOS method (100 watts)
was carried out at 60 ? for 90 minutes, resulting in a yield of 84.2%. Furthermore,
the lophine compound was used to synthesize ionic liquid (DMTPI]I) by MAOS
method (30 watts) at 30 ? for 60 minutes with a yield of 16.3%. The successfully
synthesized ionic liquid was used as a solvent to synthesize 2-oxazolidinone
compounds using MAOS method (250 watts) at 85 ? for 4 hours resulting in a yield
of 41.4%. The benzyl compound gave an IR absorption peak of aromatic C-H
vibrations at 3054 cm-1 and C=O vibrations at 1583 cm-1. The lophine compound gave
IR absorption peaks of N-H vibrations at the wavenumber of 3431 cm-1, C=N imine
vibrations at 1661 cm-1, and C-N vibrations at 1262 cm-1. The ionic liquid ([DMTPI]I)
gave IR absorption peaks of O-H vibrations at 3438 c cm-1 indicating the hydroscopic
nature of the ionic liquid, C-H sp³ vibrations at 2915 cm-1, and C-N imine at 1261 cm
1
. The ¹H-NMR measurement results for compound 2-oxazolidinone gave a typical
signal of CH2-N protons at 3,47 ppm, a typical signal of CH2-O protons at 4,25 ppm,
and a typical signal of N-H protons at 5,74 ppm. The 13C-NMR measurement results
for compound 2-oxazolidinone 158,06 ppm, 40,79 ppm, dan 65,42 ppm |
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