HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1058174Erstellt: 26. Oktober 2026
2,6-Dimethoxybenzoic Acid → Benzoic acid, 2,6-dimethoxy-, methyl ester
https://huagongshe.com/reaction/1058174
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2,6-Dimethoxybenzoic Acid | HCID 15109 | — |
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Dimethyl Carbonate | HCID 12021 | — |
| Produkt | Benzoic acid, 2,6-dimethoxy-, methyl ester | HCID 137419 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06515167B1 |
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| Quelldatensatz | uspto-grants-2003_02 |
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| ORD ID | ord-107e392ba5f74beaa591bfe07c008edd |
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| Quellennotiz | uspto-grants-2003_02 |
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