Oleralignan in portulaca oleracea as well as extraction and separation method and applications thereof
A separation method and technology of purslane, which are applied in the directions of ether separation/purification, antidote, ether preparation, etc., can solve the problem of low structural novelty, and achieve the effects of environmental protection process method, simple and fast operation method
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Embodiment 1
[0030] The present invention provides new compound, molecular formula is C 18 h 16 o 4 , named as olealignan chemical structure shown in Figure 10.
[0031] Described new compound is called olealignan according to structure, and table 1 is the NMR data of this new compound: 1 H-NMR with 13 C-NMR in deuterated DMSO.
[0032]
[0033]
[0034] The structural identification of the compounds of the present invention can be referred to Figure 1-10 .
[0035] Oleralignan: Yellow-green powder, easily soluble in methanol. After spotting the sample on the silica gel thin-layer plate, spray the ferric chloride test solution and the spot turns blue. UV(MeOH)λ max : 291,236nm. IR v max 3393,2925,2850,1600, 1515,1478,1256,1203,1159,1125,1021,859,790,762cm -1 . HRESI(+)TOFMS gives m / z: 297.1092[M+H] + The quasi-molecular ion peak has a molecular weight of 296.1043. combine 1 H-NMR, 13 According to C-NMR and DEPT data, it is speculated that the possible molecular form...
Embodiment 2
[0046] Embodiment 2 is basically the same as Embodiment 1, and its difference is:
[0047] Water is 8 times in step 1.
[0048] Step 6: Acetonitrile: 0.1% (volume percent) formic acid (48:52, v:v) was used as the mobile phase, and the detection wavelength was 210nm, 280nm, and the new compound of the present invention was obtained by separation with a purity of 93%.
Embodiment 3
[0050] Embodiment 3 is basically the same as Embodiment 1, and its difference is:
[0051] Water is 16 times in step 1.
[0052] In step 6, acetonitrile: 0.1% (volume percent) formic acid (50:50, v:v) was used as the mobile phase, and the detection wavelength was 210nm, 280nm to separate and prepare the new compound of the present invention with a purity of 90%.
[0053] Obtained from embodiment 1-3: the purity measured by normalization method is 90~97.5%.
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