Solvent free hydroxylation of the methyl esters of Blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate
© Adewuyi et al 2010
Received: 14 September 2011
Accepted: 6 December 2011
Published: 6 December 2011
Extraction of oil from the seed of Blighia unijugata gave a yield of 50.82 ± 1.20% using hexane in a soxhlet extractor. The iodine and saponification values were 67.60 ± 0.80 g iodine/100 g and 239.20 ± 1.00 mg KOH/g respectively with C18:1 being the dominant fatty acid. Unsaturated methyl esters of Blighia unijugata which had been previously subjected to urea adduct complexation was used to synthesize methyl 9, 10-dihydroxyoctadecanoate via hydroxylation in the presence of cetyltrimethylammonium permanganate (CTAP). The reaction was monitored and confirmed using FTIR and GC-MS. This study has revealed that oxidation reaction of mono unsaturated bonds using CTAP could be achieved under solvent free condition.
The replacement of petrochemicals by oleochemical feedstocks in many industrial and domestic applications as resulted in increase in demand for bio-based products and as such recognizing and increasing the benefits of using renewable materials. This has reduced the dependence on imported petroleum and promoted the sustainable agricultural initiative. Vegetable oils are one of the most versatile renewable substrates and can be converted into several products [1–3]. The use of lesser known seed oils is of great benefit in this regards, example of such lesser known underutilized seed oil is that of Blighia unijugata.
Blighia unijugata is a tree planted as shade tree in Nigeria. It is of attractive appearance especially when in fruit which are red or pinkish yellow. The wood is used for buildings; it is also recognized for its sedative and analgesic properties in treatment of rheumatism . Presently, the seed oil has no specific use in Nigeria as the seeds are discarded as waste.
Natural polyols can be obtained by chemical modification of the vegetable oils introducing hydroxyl groups in an unsaturated triglyceride by hydroxylation of carbon-carbon double bonds and/or by alcoholysis of the triglyceride to obtain mainly a monoglyceride [3, 5]. Vegetable oil contains mixture of different unsaturated and saturated fatty acids in varying amounts; these have different applications, though, there is little or scanty report on their isolation.
Urea complexation reaction is a well-established technique for elimination of saturated and monounsaturated fatty acids [6–9]. Urea complexation has the advantage that complexed crystals are extremely stable, and filtration does not necessarily have to be carried out at the very low temperatures which solvent crystallization of fatty acids would require. This method is also favorable because complexation depends upon the configuration of the fatty acid moieties due to the presence of multiple double bonds, rather than pure physical properties such as melting point or solubility . The saturated and monounsaturated fatty acids easily complex with urea and crystallize out on cooling and may subsequently be removed by filtration. The liquid or non-urea complexed fraction is enriched with unsaturated fatty acids.
The fundamentally attractive concept of green Chemistry is solvent free reactions. Solvent-free reactions are an interesting alternative approach, mainly when these conditions eliminate the use of a solid support or solvent from the reaction . A dry solid-phase reaction is solvent-free, also a reaction where there is liquid presence, but not acting as a solvent (i.e. nothing is dissolved in it) is also solvent-free" . The economic benefits of green Chemistry are central drivers in its advancement. Industry is adopting green Chemistry methodologies because they improve the corporate bottom line. A wide array of operating costs is decreased through the use of green Chemistry. When less waste is generated, environmental compliance casts go down and when waste is eliminated treatment and disposal become unnecessary. Decreased solvent usage and fewer processing steps lessen the material and energy costs of manufacturing and increase material efficiency.
Permanganate, an important oxidant in many organic and inorganic redox reactions, involves the Mn (VII) entity, which is renowned for its versatility. The permanganate oxidation process is eco-friendly and has gained importance in green Chemistry. Cetyltrimethylammonium permanganate (CTAP) possess a long hydrocarbon chain that can draw substrate close to MnO4- ion in a micelle-like aggregation, thereby enabling reactant molecules to efficiently interact with oxidizing ion even if a homogenizing solvent is not present. This attribute pointed our attention to the hydroxylation of olefin bonds in the unsaturated methyl esters from seed oil of Blighia unijugata with cetyltrimethylammonium permanganate. In the present study, the seed oil of Blighia unijugata was chemically characterized, the unsaturation of the methyl ester was increased using urea adduct complexation reaction and 9,10-dihydroxyoctadecanoate was synthesized from the unsaturated methyl esters using cetyltrimethylammonium permanganate.
Materials and method
Extraction and chemical analysis of the seed oil of Blighia unijugata
The dried seeds of Blighia unijugata were extracted with n-hexane for 10 hr using soxhlet extractor . The oil was analyzed for iodine, saponification and free fatty acid content by method described by the Association of Official Analytical Chemist .
Fatty acid composition of Blighia unijugata
Fatty acid methyl esters of the oil were prepared by refluxing the sample at 70°C for 3 h in 2% sulphuric acid in methanol. The esters were extracted into ethyl acetate, washed free of acid and passed over anhydrous sodium sulphate. The ethyl acetate extracts were further concentrated using a rotary evaporator. The fatty acid composition was analyzed using an Agilent 6890 N series gas chromatography equipped with FID detector on a split injector. A fused silica capillary column (DB-225, 30 × 0.32 m i.d., J & W Scientifics, USA) was used with the injector and detector temperature maintained at 230°C and 250°C respectively. The oven temperature was programmed at 160°C for 2 min and finally increased to 230°C at 4°C/min. The carrier gas was nitrogen at a flow rate of 1.5 mL/min. The area percentages were recorded with a standard Chemstation Data System.
Urea adduct complexation reaction of Blighia unijugata methyl esters
Fatty acid methyl esters for the urea adduct complexation reaction were prepared by refluxing the oil at 70°C for 3 h in 1% KOH in methanol. The esters were extracted into ethyl acetate, washed free of acid and passed over anhydrous sodium sulphate. The ethyl acetate extracts were further concentrated using a rotary evaporator. Methyl esters (100 g) were dissolved in methanol (1000 ml) to which urea (200 g) had been added. The mixture was warmed with stirring until the whole mixture turned into a clear homogeneous solution . The solution was allowed to cool to room temperature and kept refrigerated at 5°C for 8 h. Crystals were removed by filtering through a Buchner funnel to remove the urea complexes, which were washed twice with 25 ml of methanol saturated with urea. The filtrate which is rich in unsaturated methyl esters was poured into 1% hydrochloric acid (600 ml) and extracted alternatively with hexane and diethyl ether. The combined organic layers were washed with water twice (50 ml) and passed over anhydrous sodium sulphate and later concentrated using a rotary evaporator. This reaction was repeated changing the ratio of fatty acid methyl esters to urea from 1:2 to 2:1 in order to further increase the unsaturation of the methyl esters. The resulting methyl esters (BME) were then taken for the determination of the constituent fatty acids using a GC as described above.
Preparation of cetyltrimethylammonium permanganate
This was achieved by introducing a solution of 27.0 mmol of KMnO4 (4.25 g in 25 ml distilled water) into a 250 ml two-necked round bottom flask in a water bath maintained at 8°C. After about 15 min, solution of 25.0 mmol of cetyltrimethylammonium bromide (9.10 g in 50 ml dichloromethane) was added into the flask and stirred for 4 h. The organic layer was separated and the solvent recovered under reduced pressure with the crystalline cetyltrimethylammonium permanganate (purple coloured) precipitating out before the complete recovery of the solvent; it was filtered, washed with distilled water and ether and dried over P2O5 under vacuum.
Dihydroxylation of BME using cetyltrimethylammonium permanganate
The dihydroxylation was carried out in a clamped three necked round bottom flask equipped with a thermometer and a stirrer in a thermo-regulated water bath. About 2.10 g (5.2 mmol) of cetyltrimethylammonium permanganate with five drops of distilled water was introduced into the flask. About 5.0 mmol of BME was slowly added drop wise while stirring the mixture. The mixture was stirred for 1 h and extracted three times with 50 ml portion of ether; this was later washed with saturated solution of NaCl, dried over Na2SO4 and concentrated on a rotary evaporator.
Isolation of methyl 9, 10-dihydroxyoctadecanoate
The final product was separated on a 1 g scale by silica gel column chromatography using a glass column 20 cm × 2 cm OD packed with 30 g activated silica gel (60-120 mesh). Hydrocarbons and other non-polar compounds were eluted with petroleum ether (boiling point, 60-80°C). The methyl 9, 10-dihydroxyoctadecanoate were eluted using a mixture of petroleum ether - diethyl ether (40:60 v/v). The fractions were screened by TLC for the identification of the compounds isolated. The eluted spots were identified using iodine vapors.
Trimethylsilylation derivatisation and GC-MS analysis of methyl 9, 10-dihydroxyoctadecanoate
The isolated methyl 9,10-dihydroxyoctadecanoate was derivatised and identified by GC-MS analysis using Agilent (Palo Alto, USA) 6890 N gas chromatography equipped with an HP-1 MS capillary column connected to an Agilent 5973 mass spectrometer operating in the EI mode (70 ev; m/z 50-550; source temperature 230°C and quadruple temperature 150°C). Methyl 9,10-dihydroxyoctadecanoate was silylated using N, O-Bis(trimethylsilyl)trifluoroacetamide; about 13 μl/mg of N, O-Bis(trimethylsilyl)trifluoroacetamide was added to methyl 9,10-dihydroxyoctadecanoate, kept at 75°C for 60 min and thoroughly shaken. The final product was extracted in ethyl acetate and concentrated using a rotary evaporator. Structural assignments were made based on interpretation of mass spectrometric fragmentation and confirmation by comparison of retention time as well as fragmentation pattern of authentic compounds and the spectral data obtained from the Wiley and NIST libraries.
Fourier Transform Infrared (FTIR)
The FTIR spectra of the methyl esters and hydroxylated methyl esters were recorded using a Perkin Elmer FTIR system spectrum BX LR64912C. The samples were spread over NaCl cells, and their spectra were recorded in the range of 4000-400 cm-1.
Results and discussion
Chemical characterization and fatty acid composition of the seed oil of Blighia unijugata
Characterization of the oil of B.unijugata
Oil yield (%)
50.82 ± 1.20
7.00 ± 0.1
Iodine value (g iodine/100 g)
67.60 ± 0.80
Saponification value (mg KOH/g)
239.20 ± 1.00
Fatty acid composition (wt %) of B.unijugata
0.2 ± 0.10
34.5 ± 0.20
14.1 ± 0.10
48.1 ± 0.50
1.8 ± 0.30
0.3 ± 0.20
0.5 ± 0.10
0.2 ± 0.00
0.3 ± 0.10
50.4 ± 0.20
49.6 ± 0.10
Urea adduct complexation reaction of Blighia unijugata methyl esters
Dihydroxylation of BME using cetyltrimethylammonium permanganate
Isolation and GC-MS analysis of methyl 9, 10-dihydroxyoctadecanoate
Oil was extracted from the seed of Blighia unijugata using hexane in a soxhlet extractor. The iodine value was 67.60 ± 0.80 g iodine/100 g while the saponification value was 239.20 ± 1.00 mg KOH/g. The dominant fatty acid was found to be C18:1. The unsaturation of the methyl esters of Blighia unijugata was increased using the urea adduct complexation reaction. Methyl 9, 10-dihydroxyoctadecanoate was synthesized from the methyl esters via hydroxylation using cetyltrimethylammonium permanganate. The reaction was monitored and confirmed using FTIR and GC-MS. This study has revealed that oxidation reaction using CTAP do not require solvent medium and can be achieved under complete solvent free condition.
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