HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785211Generated: October 30, 2026
Methyl Acrylate → 3-(2-Methyl-4-nitro-phenyl)-acrylic Acid Methyl Ester
https://huagongshe.com/reaction/1785211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Bromo-2-methyl-4-nitrobenzene | HCID 251672 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Propionitrile | HCID 7854 | — |
| Product | 3-(2-Methyl-4-nitro-phenyl)-acrylic Acid Methyl Ester | HCID 68839650 | 91.1% |
Reaction Steps
To a solution of 2-bromo-5-nitrotoluene (3.11 g, 14.39 mmol) in propionitrile (105 mL) is added DIPEA (5.1 mL, 29.28 mmol). The mixture is degassed three times. Methyl acrylate (5.2 mL, 57.74 mmol) is added and the mixture is degassed. Tri-o-tolylphosphine (1.77 g, 5.82 mmol) and Pd(OAc)2 (0.64 g, 2.85 mmol) are added and the mixture is degassed a final two times followed by heating at 110° C. for 4 h. Upon cooling, the mixture is passed through Celite and the filtrate is concentrated. The residue is partitioned between Et2O and 1N HCl. The organics are washed with saturated NaHCO3 and brine, and dried with Na2SO4. The crude material is purified by flash chromatography to yield the title compound (2.90 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504433B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-d9d4c8f34da04b73ae6b70991b0b57d6 |
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| Source note | uspto-grants-2009_03 |
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