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Contact Name
Muhammad Syahrir
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m.syahrir7406@unm.ac.id
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nurkhasanah@pharm.uad.ac.id
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Jl. Prof. Dr. Soepomo, S.H., Janturan, Warungboto, Umbulharjo, Yogyakarta, Indonesia Kode pos 55164
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INDONESIA
Pharmaciana: Jurnal Kefarmasian
ISSN : 20884559     EISSN : 24770256     DOI : 10.12928
Core Subject : Health,
Pharmaciana is a scientific journal published by the University of Ahmad Dahlan worked closely with Ikatan Apoteker Indonesia (IAI). Pharmaciana published three times a year, namely March, July and November. with ISSN 2088-4559 and e-ISSN 2477-0256. The article published in the Journal Pharmaciana selected by editors and reviewed by the reviewer. Articles published in Pharmaciana must not be published in other journals or have been previously published. Pharmaciana is indexed in google scholar, ACI (Asean Citation Index), Dimension (Crossreff), Garuda, Sinta, Sherpa Romeo, Index Copernicus International, DOAJ, and BASE. Pharmaciana is accredited by DIKTI (DGHE) of Indonesia No. 105/E/KPT/2022 April 07, 2022
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Search results for , issue " Vol 5, No 1 (2015): Pharmaciana Vol 5 No 1, 2015" : 1 Documents clear
SINTESIS 4–HIDROKSI–3–KLOROBENZALDEHID DARI p–HIDROKSIBENZALDEHID DAN GAS Cl2 Warsi, Warsi
PHARMACIANA Vol 5, No 1 (2015): Pharmaciana Vol 5 No 1, 2015
Publisher : Universitas Ahmad Dahlan

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Abstract

ABSTRAK Kurkumin merupakan senyawa yang potensial untuk dikembangkan. Senyawa analog kurkumin telah banyak disintesis. Senyawa 4–hidroksi–3–klorobenzaldehid merupakan bahan dasar dalam sintesis analog kurkumin dengan substituen –Cl pada inti aromatiknya. Senyawa4–hidroksi–3–klorobenzaldehid telah disintesis melalui reaksi klorinasi antara p–hidroksibenzaldehid dan gas Cl2, kemurnian 4–hidroksi–3–klorobenzaldehid ditentukan berdasarkan jarak lebur, kromatografi lapis tipis dan LC–MS. Identifikasi struktur senyawa hasil sintesis dilakukan dengan teknik spektrometri, meliputi spektramassa (ESI–MS), spektra inframerah (cm-1, KBr), spektra resonansi magnetik inti proton (δ, ppm, DMSO–d6, 1H–NMR, 500 MHz) dan UV–Vis. Reaksi klorinasi p–hidroksibenzaldehid dihasilkan 4–hidroksi–3–klorobenzaldehid yang berbentuk kristal warna kuning, dengan jarak lebur 128,1–130,8ºC. Rendemen rata–rata yang dihasilkan sebesar 51,37 %.Kata kunci: 4–hidroksi–3–klorobenzaldehid, klorinasi, halogenasi

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