SYNTHESIS OF 4-ALLYL-2-METHOXY-6-AMINOPHENOL FROM NATURAL EUGENOL Sintesis 4-AIIII-2-metoksl-6-amlnofenol darl Senyawa Bahan Alam Eugenol
ABSTRACT The aim of this preliminary research was to synthesize derivatives of eugenol such as 4-al/yl-2-methoxy-6- nitrophenol (2) and 4-al/yl-2-methoxy-6-aminophenol (3). The result could be used as a reference on the transformation of eugenol to its derivatives. Theoriticaly nitration of eugenol...
محفوظ في:
المؤلف الرئيسي: | |
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التنسيق: | مقال NonPeerReviewed |
منشور في: |
[Yogyakarta] : Universitas Gadjah Mada
2008
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الموضوعات: | |
الوصول للمادة أونلاين: | https://repository.ugm.ac.id/27974/ http://i-lib.ugm.ac.id/jurnal/download.php?dataId=11037 |
الوسوم: |
إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
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المؤسسة: | Universitas Gadjah Mada |
الملخص: | ABSTRACT
The aim of this preliminary research was to synthesize derivatives of eugenol such as 4-al/yl-2-methoxy-6-
nitrophenol (2) and 4-al/yl-2-methoxy-6-aminophenol (3). The result could be used as a reference on the
transformation of eugenol to its derivatives. Theoriticaly nitration of eugenol (1) by nitric acid could produced 4-al/yl-
2-methoxy-6-nitrophenol (2) and fol/owed by reduction could achieved 4-al/yl-2-mehtoxy-6-aminophenol (3). The
formation of this product was analyzed by analytical thin layer chromatography (TLC) and GC-MS. These analysis
showed the formation of product (2) and (3) were visible. TLC showed product (1) less polar than eugenol and gave
orange colour, and supported by GC-MS which showed molecular ion at f!l/z 209 due to the presenceof -N02 by
replacing one H at 6 position of eugenol. Product (3) was afforded by reduction of (2) with Sn/HCI and tIc analysis
showed compound (3) more polar than eugenol (1) and (2) and supported by GC-MS which showed molecular ion at
m/z 179 due to the presence of -NH2. |
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