HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968457Generated: October 29, 2026
Ethyl Acetate → Methyl 2-(2,4-dimethoxyphenyl)-5-nitrobenzoate
https://huagongshe.com/reaction/1968457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Methyl 2-Bromo-5-nitrobenzoate | HCID 245494 | — |
| Reactant | 2,4-Dimethoxybenzeneboronic acid | HCID 2734341 | — |
| Catalyst | HCID 178419050 | HCID 178419050 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(2,4-dimethoxyphenyl)-5-nitrobenzoate | HCID 57990576 | — |
Reaction Steps
A mixture of 2,4-dimethoxyphenylboronic acid (25.0 g, 137 mmol), methyl 2-bromo-5-nitrobenzoate (35.7 g, 137 mmol), cesium carbonate (89.4 g, 274 mmol) and bis(triphenylphosphine)palladium (II) dichloride (4.81 g, 6.85 mmol) was suspended in N, N-dimethylformamide (450 mL), and then stirred under argon atmosphere at 80° C. overnight. After cooling down, ethyl acetate (200 mL), diethylether (400 mL) and water (1000 mL) were added thereto, and then separated. The water layer was extracted with a mixed solvent of ethyl acetate (150 mL)-diethylether (150 mL) (twice). The organic layer was combined and washed with water (500 mL, 3 times) and saturated brine (500 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure to give the titled reference compound as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426406B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-a33a5b7b182d42388348cb8883de3910 |
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| Source note | uspto-grants-2013_04 |
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