HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058174Generated: October 26, 2026
2,6-Dimethoxybenzoic Acid → Benzoic acid, 2,6-dimethoxy-, methyl ester
https://huagongshe.com/reaction/1058174
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dimethoxybenzoic Acid | HCID 15109 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethyl Carbonate | HCID 12021 | — |
| Product | Benzoic acid, 2,6-dimethoxy-, methyl ester | HCID 137419 | — |
Reaction Steps
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), (836 mg, 5.49 mmol), was added to a mixture of 2,6-dimethoxybenzoic acid (1), (1.0 g, 5.49 mmol), in dimethyl carbonate (DMC) (10 mL) and the resulting mixture was heated to reflux at 90° C. for 4 hours. The reaction mixture was cooled to 25° C. and diluted with EtOAc (30 mL) and water (30 mL). The organic layer was separated and washed in sequence with 10 mL of water, 2 M HCl (2×30 mL), saturated aqueous NaHCO3 (2×30 mL) and water (2×25 mL). The organic layer was dried over Na2SO4, filtered and concentrated under vacuum to give methyl 2,6-dimethoxybenzoate (2) as a white solid. The yield of the 2,6-dimethoxybenzoate as determined by HPLC was 97-98% conversion.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515167B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-107e392ba5f74beaa591bfe07c008edd |
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| Source note | uspto-grants-2003_02 |
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