Table 2.
1H and 13C NMR assignments for syringic acid and its derivatives 2, 5 and 6a
Position |
Syringic acid |
2 |
5 |
6 |
||||
---|---|---|---|---|---|---|---|---|
δCb | δH (m, J Hz) | δCb | δH (m, J Hz) | δCc | δH (m, J Hz) | δCb | δH (m, J Hz) | |
1 |
128.6, C |
- |
121.1, C |
- |
121.1, C |
- |
121.0, C |
- |
2 |
107.0, CH |
7.31 (s) |
106.8, CH |
7.36 (s) |
106.9, CH |
7.35 (s) |
106.8, CH |
7.38 (s) |
3 |
148.0, C |
- |
146.7,C |
- |
146.7, C |
- |
146.6, C |
- |
4 |
142.6, C |
- |
139.4, C |
- |
139.4, C |
- |
139.4, C |
- |
5 |
148.0, C |
- |
146.7, C |
- |
146.7, C |
- |
146.6, C |
- |
6 |
107.0, CH |
7.31 (s) |
106.8, CH |
7.36 (s) |
106.9, CH |
7.35 (s) |
106.8, CH |
7.38 (s) |
1' |
- |
- |
136.3, C |
- |
137.9, C |
- |
136.5, C |
- |
2' |
- |
- |
128.2, CH |
7.45 (dd, 7.8, 1.2) |
113.8d, CH |
6.98 (d, 2.2) |
105.9, CH |
6.59 (d, 2.4) |
3' |
- |
- |
128.6, CH |
7.39 (dd, 7.8, 7.2) |
160.0, C |
- |
160.9, C |
- |
4' |
- |
- |
128.2, CH |
7.34 (dd, 7.2, 1.2) |
113.7d, CH |
6.88 (dd, 8.1, 2.2) |
100.0, CH |
6.45 (dd, 2.4, 2.4) |
5' |
- |
- |
128.6, CH |
7.39 (dd, 7.8, 7.2) |
129.8, CH |
7.30 (dd, 10.0, 8.8) |
160.9, C |
- |
6' |
- |
- |
128.2, CH |
7.45 (dd, 8.8, 1.2) |
120.4, CH |
7.02 (d, 7.7) |
105.9, CH |
6.59 (d, 2.4) |
7'-CH2 |
- |
- |
66.7, CH2 |
5.36 (s) |
66.8, CH2 |
5.32 (s) |
66.5, CH2 |
5.30 (s) |
3,5-OCH3 |
56.1, CH3 |
3.86 (s) |
56.5, CH3 |
3.93 (s) |
56.6, CH3 |
3.93 (s) |
56.5, CH3 |
3.95 (s) |
3'-OCH3 |
- |
- |
- |
- |
55.3, CH3 |
3.82 (s) |
55.4, CH3 |
3.82 (s) |
5'-OCH3 |
- |
- |
- |
- |
- |
- |
55.4, CH3 |
3.82 (s) |
OH | - | 4.93 (s) | - | 5.92 (s) | - | 5.91 (br s) | - | 5.95 (s) |
aSpectra recorded in CDCl3. bMultiplicities were determined by DEPT 135. cMultiplicities were determined by APT. dAssignments may be interchanged.