Extraction method of phenolic compounds in lepidium latifolium and phenolic compounds extracted by extraction method
A technology of phenolic compounds and extraction methods, which is applied in the field of compound extraction from Lipeacea broadleaf, can solve the problems of extracting phenolic components of Lipega broadleaf, restricting the utilization and research of Lipega broadleaf, and achieves stable and controllable quality, Easy batch preparation and simple preparation process
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Embodiment 1
[0041] A kind of extracting method of phenolic acid compounds in unifoliate japonica, comprising the following steps:
[0042] S1. Take 20kg of lentils, dry them at 55°C for 4 days, and then pulverize them to obtain 40-mesh coarse powder;
[0043] S2, extract the coarse powder in step S1 with 95wt% ethanol under ultrasonic conditions of 40KHz and 600W for 3 times, each time for 1h, and mix the obtained extracts, then concentrate under reduced pressure at 65°C and 150hpa for 20min to obtain 1.8kg of extract;
[0044] S3, adding 100kg of water to the medicinal extract in step S2 for dispersion, then adding 100kg of petroleum ether for extraction to obtain 72.6g of extract;
[0045] S4. The extract obtained in step S3 was concentrated under reduced pressure at 65° C. and 150 hpa for 20 minutes to obtain 35 g of extract, which was eluted with a silica gel column eluent after silica gel column chromatography, and the silica gel column eluent was A mixture of dichloromethane, meth...
Embodiment 2
[0050] The difference from Example 1 is that in step S3, adding 100 kg of petroleum ether for extraction is changed to adding 100 kg of ethyl acetate to obtain syringic acid.
[0051] The obtained syringic acid is carried out structural identification, and the identification results are as follows:
[0052] Compound spectral data: syringic acid is a white powder. Molecular formula C 9 h 10 o 5 , 1 H NMR(600MHz,MEOD)δ:7.33(2H,s,H-2,H-6),3.88(6H,s,3,5-OCH 3 ); 13 C-NMR(600MHz,MEOD)δ:168.7(s,C-7),147.4(s,C-3,C-5),140.3(s,C-4),120.7(s,C-1), 106.9(s,C-2,C-6),55.4(s,3,5-OCH 3 ).
Embodiment 3
[0054] The difference from Example 1 is that in step S3, adding 100 kg of petroleum ether for extraction is changed to adding 100 kg of n-butanol to obtain p-hydroxycinnamic acid.
[0055] Spectral data of the compound: p-Hydroxycinnamic acid is white crystal. Molecular formula C 9 h 8 o 3 , 1 H NMR (600MHz, MEOD) δ: 7.60 (1H, d, J = 15.9Hz, H-7), 7.45 (2H, d, J = 8.6Hz, H-3, 5), 6.80 (2H, d, J =8.6Hz,H-2,6),6.28(1H,d,J=15.9Hz,H-8); 13 C-NMR(600MHz,MEOD)δ:169.6(s,C-9),159.8(s,C-1),145.2(s,C-7),129.7(s,C-3,5),125.8( s, C-4), 115.4 (s, C-2, 6), 114.2 (s, C-8).
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