Products distribution of other phenolics compounds at different temperaturesa.
| Reactant | Phenol | Anisole | Phenol | Anisole |
| Temperature | 300 | 300 | 400 | 400 |
| Conversion (%) | ||||
| Phenol | 63.34 | — | 99.28 | — |
| Anisole | — | 59.4 | — | 98.7 |
| Yield (%) | ||||
| PMB | 4.38 | 3.68 | 10.19 | 8.99 |
| HMB | 2.87 | 2.74 | 52.45 | 49.76 |
| Methylated anisole | — | 10.72 | — | — |
| Mesitylene | — | — | 0.71 | 0.82 |
| Benzene, 1,2,4,5-tetramethyl | — | — | 1.68 | 0.79 |
| Benzene, 1,2-diethyl-3,4-dimethyl | — | — | 2.07 | 3.32 |
| Phenol | — | 8.83 | — | — |
| Anisole | 7.6 | — | — | — |
| Guaiacol | — | 2.38 | — | — |
| Phenol, 2,6-dimethyl- | 7.12 | 3.89 | 0.76 | 1.42 |
| Phenol, 2,4,6-trimethyl- | 10.35 | 3.56 | — | 1.27 |
| Phenol, 2,3,5,6-tetramethyl | 5.54 | 2.83 | 0.52 | 0.23 |
| Phenol, 2-(1,1-dimethylethyl)-3-methyl | 8.32 | 6.54 | 1.42 | — |
Reaction condition: catalyst = 33-SA, N2 = 50 mL min−1, WHSV = 4 h−1, methanol to phenolic compounds molar ratio = 25.