HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13896Generated: October 26, 2026
Methyl Methacrylate → methyl (2E)-3-[4-(dimethylamino)phenyl]-2-methylprop-2-enoate
https://huagongshe.com/reaction/13896
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | 4-bromo-N,N-dimethylaniline | HCID 11465 | — |
| Reactant | alpha-Cyclohexylcyclohexanemethanamine | HCID 10774245 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | Tri-tert-butylphosphonium tetra-para-tolylborate | HCID 23136639 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl (2E)-3-[4-(dimethylamino)phenyl]-2-methylprop-2-enoate | HCID 11390367 | 87% |
Reaction Steps
A 30-ml four-necked flask was equipped with a stirrer, a thermometer and a reflux condenser. 1.000 g (5 mmol) of 4-dimethylaminobromobenzene, 1.001 g (10 mmol) of methyl methacrylate, 0.011 g (0.012 mmol) of tris(dibenzylideneacetone)dipalladium (0), 1.074 g (5.5 mmol) of dicyclohexylmethylamine and 5 ml of tetrahydrofuran were weighed in the flask, followed by stirring. Further, 0.029 g (0.05 mmol) of tri-tert-butylphosphonium tetra-para-tolylborate obtained in Example B-3 was weighed in air and added into the flask. The flask was purged with argon, followed by stirring at 30° C. for 25 hours. After the completion of the reaction, 5 ml of toluene and 10 ml of saturated sodium chloride solution were added, followed by separation. The organic phase was purified by column chromatography to afford 0.954 g of (E)-3-(4-dimethylaminophenyl)-2-methylacrylic acid methyl ester (yield: 87 mol % based on 4-dimethylaminobromobenzene). The identification of the product was made by H-NMR and 3C-NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07728176B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-b0ed96f2a095420cbe1c0169339b4132 |
|---|
| Source note | uspto-grants-2010_06 |
|---|