“…In the 1 H NMR spectrum, two groups of aromatic protons signals at δ 7.49 (1H, dd, J = 1.9, 8.3 Hz), δ 7.45 (1H, d, J = 1.9 Hz), δ 6.90 (1H, d, J = 8.3 Hz), and δ 6.78 (1H, dd, J = 1.6, 8.2 Hz), δ 6.74 (1H, d, J = 8.2 Hz) and δ 6.91 (1H, d, J = 1.6 Hz) appeared as two ABX coupling systems, which belonged to two 1, 3, 4-tri-substituted aromatic rings. The 13 C NMR data of 2 were most close to those of 3-methoxy-4-hydroxyphenylpropane-7, 8-(6′-benzoyl-2′, 1′-O-β-glucopyranosyl)-7, 8, 9-triol (Truong et al, 2011), except the signals of C-3′′ and C-4′′ of 2, which are down-field by 18 and 17 ppm, respectively, indicating an ortho-dioxide substitution at 3′′ and 4′′ in 2. Their substitution position were further confirmed by the long-range correlations between δ 3.83(-OCH3) and δ 147.3(C-3′′), δ 9.03(-OH) and δ 151.7(C-4′′), and δ 7.49(H-6′′) and δ 151.7(C-4′′) in the HMBC experiment.…”