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A long chain alcohol as support in solid phase organic synthesis
Nurlela, Yeni1, Minnaard, Adrian J2, Achmad, Sadijah3, Wahyuningrum, Deana4.
The solid phase synthesis is a method by which organic compound synthesis are performed on a support. With this method, the purification can be carried out easily by simple filtration and washing procedures. Long-chain alcohol (C-100 alcohol) can be used as a support because of its insolubility in organic solvents and its simple structure which enables it to be stable in various reaction conditions. In this study, a 4-aminopyridine derivative has been synthesized from C-100 β-keto ester and a cyano enamine using tin(VI)chloride as catalyst. C-100 β-keto ester was obtained by transesterification of long chain alcohol (the support) with ethyl acetoacetate using boric acid protocol. The cyano enamine was successfully synthesized by Thorpe-Ziegler cyclization initiated by sodium hydride. The 4-aminopyridine derivative was successfully cleaved from the support using sodium isopropoxide in refluxing isopropanol. From the 1H-NMR spectrum at ~ 120oC, it was found that the cleaved support has the same spectrum with the long-chain alcohol used in the beginning of reaction, thus, this long chain alcohol can be reused for other reactions.
Affiliation:
- Institut Teknologi Bandung, Indonesia
- Institut Teknologi Bandung, Indonesia
- Institut Teknologi Bandung, Indonesia
- University of Groningen, Netherlands
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Indexation |
Indexed by |
MyJurnal (2021) |
H-Index
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6 |
Immediacy Index
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0.000 |
Rank |
0 |
Indexed by |
Web of Science (SCIE - Science Citation Index Expanded) |
Impact Factor
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JCR (1.009) |
Rank |
Q4 (Multidisciplinary Sciences) |
Additional Information |
JCI (0.15) |
Indexed by |
Scopus 2020 |
Impact Factor
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CiteScore (1.4) |
Rank |
Q2 (Multidisciplinary) |
Additional Information |
SJR (0.251) |
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