HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49691Generated: October 25, 2026
2,6-Dimethoxyphenol → 1,2,3-Trimethoxybenzene
https://huagongshe.com/reaction/49691
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dimethoxyphenol | HCID 7041 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,2,3-Trimethoxybenzene | HCID 12462 | — |
Reaction Steps
To a solution of 2,6-dimethoxyphenol (1.0 g, 6.49 mmol) in DMC (10 mL), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (0.99 g, 6.49 mmol) was added and the resulting solution was heated to reflux (90° C.) for 4.5 hours. The reaction was cooled to ambient temperature and diluted with EtOAc (50 mL) and H2O (40 mL). The organic layer was separated and washed in sequence with H2O (40 mL), 2M HCl (2×40 mL), 2M NaOH (2×40 mL) and H2O. The organic layer was dried over Na2SO4, filtered and concentrated under vacuum to give trimethoxybenzene as a solid. The yield of trimethoxybenzene as determined by HPLC was 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706929B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-74f981d105f24b61a718cb4381b6bd64 |
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| Source note | uspto-grants-2004_03 |
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