HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398166Generated: October 29, 2026
Ethyl Acetate → Methyl 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoate
https://huagongshe.com/reaction/1398166
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Methyl 4-[formyl-(2-oxopropyl)amino]-3-methoxybenzoate | HCID 86602464 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoate | HCID 27282443 | 52.9% |
Reaction Steps
A mixture of methyl 4-[formyl(2-oxopropyl)amino]-3-methoxybenzoate (32.6 g) and ammonium acetate (47.5 g) in acetic acid (65.6 mL) was stirred at 140° C. for 1 hr. After completion of the reaction, ethyl acetate and saturated aqueous sodium hydrogen carbonate solution were added under ice-cooling, and the organic layer was separated. To the aqueous layer was added ethyl acetate, and the organic layer was separated. The organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (methanol/ethyl acetate/hexane) to give the title compound (16.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901309B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-83eec42e91884b32a63ec8e9712e1a11 |
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| Source note | uspto-grants-2014_12 |
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