A kind of refining method of thymol
A technology of thymol and a refining method, which is applied in the field of medicine and chemical industry, can solve the problems of impurities such as citronellal and isopulegol, and achieve the effects of improving product purity, simple refining method, and reducing refining cost
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Embodiment 1
[0035] In a 1000ml three-necked flask, add 250g of technical grade thymol, add 200ml of n-hexane solvent, introduce nitrogen to replace the air in the reaction flask, under nitrogen protection, turn on stirring, heat up to 70±3°C, keep stirring for 0.5 hours to make thymol Fully dissolve and clear; add activated carbon 2.5g, keep heat for decolorization for about 1h; filter, cool the filtrate naturally, slowly stir until granular solids are precipitated on the wall of the reaction vessel, adjust the stirring speed, keep stirring for about 1h, and precipitate a large amount of crystalline solids ( about 40°C), cooled to 5°C, kept stirring for 4 hours for crystallization, filtered to obtain 233g of pure white product, and dried to obtain 214g of white transparent crystalline powder solid.
Embodiment 2
[0037]In a 1000ml three-necked flask, add 250g of technical grade thymol, add 250ml of n-heptane solvent, and replace the air in the reaction flask with nitrogen. The brain was fully dissolved and clear; 5.0 g of activated clay was added, and the decolorization was maintained for about 30 minutes; filtered, the filtrate was naturally cooled, and slowly stirred until granular solids were precipitated on the wall of the reaction vessel. The solid (about 40°C) was cooled to 3°C, kept stirring for 2 hours for crystallization, filtered to obtain 231g of pure white product, and dried to obtain 206g of white transparent crystalline powder solid.
Embodiment 3
[0039] In a 1000ml three-necked flask, add 250g of technical grade thymol, add 250ml of n-octane solvent, and replace the air in the reaction flask with nitrogen. The brain was fully dissolved and clear; 2.0 g of chromatographic silica gel powder was added, and the decolorization was maintained for about 1 h; filtered, the filtrate was cooled naturally, and slowly stirred until granular solids were precipitated on the wall of the reaction vessel, and the stirring speed was adjusted. Crystalline solid (about 40°C), cooled to 1°C, kept stirring for 6 hours, filtered to obtain 248g of pure white product, and dried to obtain 186g of white transparent crystalline powder solid.
[0040] The components of the white transparent crystalline powder solids obtained in Examples 1-3 of the present invention were analyzed, and the results are shown in Table 1.
[0041] Component analysis method:
[0042] Detection instrument: gas chromatograph, Shimadzu GC-2030
[0043] Detector: FID
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