HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043669Generated: November 1, 2026
Ethyl Acetate → Methyl 2-(2,4-dimethoxyphenyl)-5-nitrobenzoate
https://huagongshe.com/reaction/1043669
Participants
| Role | Name | HCID | Charge |
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| 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 the suspension was 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 the mixture was separated into a water phase and an organic layer. The water layer was extracted with a mixed solvent of ethyl acetate (150 mL)-diethylether (150 mL) (twice). The combined organic layer was 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. (Quantitative)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563551B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-f21fadbd4674424b885ffca0e7fa6d90 |
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| Source note | uspto-grants-2013_10 |
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