Novel preparation method of fatty acid plant sterol esters
A technology of phytosterol esters and phytosterols, which is applied in the solvent-free field of synthesizing fatty acid phytosterol esters using micellar catalysts, can solve the problems of poor solubility and bioavailability, unsuitable for use in the food industry, and low enzyme catalytic efficiency. The effect of low requirements on reaction conditions, easy purification of products, and simple process
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Embodiment 1
[0028] Weigh 17.4g of hexanoic acid and add it into a reaction flask equipped with stirring and oil bath for temperature control, blow in nitrogen, heat, and then add 50g of phytosterol and 1.0mol% copper dodecyl sulfate. The reaction temperature was controlled at 80° C., and the reaction process was monitored in real time by thin-layer chromatography. Samples were taken every 0.5 h, and the reaction was performed for 3 h. Separation and purification to obtain phytosterol hexanoate.
Embodiment 2
[0030] Weigh 19.5g of octanoic acid and add it into a reaction flask equipped with stirring and temperature control in an oil bath, feed nitrogen, heat, and then add 50g of phytosterol and 1.2mol% zinc lauryl sulfate. The reaction temperature was controlled at 90° C., and the reaction process was monitored in real time by thin-layer chromatography. Samples were taken every 0.5 h, and the reaction was performed for 3 h. Separation and purification to obtain octanoic acid phytosterol ester.
Embodiment 3
[0032] Weigh 30g of lauric acid and add it into a reaction flask equipped with stirring and oil bath temperature control, feed nitrogen, heat, then add 50g phytosterol and 1.5mol% copper dodecyl sulfate. The reaction temperature was controlled at 100° C., and the reaction process was monitored in real time by thin-layer chromatography. Samples were taken every 0.5 h, and the reaction was carried out for 4 h. Separation and purification to obtain phytosterol laurate.
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