HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822274Generated: October 27, 2026
Cesium carbonate → 3-[4-(4-Bromo-phenoxy)-2-methyl-phenyl]-propionic acid methyl ester
https://huagongshe.com/reaction/1822274
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Bromo-4-iodobenzene | HCID 11522 | — |
| Reactant | 2,2,6,6-Tetramethyl-3,5-heptanedione | HCID 70700 | — |
| Reactant | Methyl 3-(4-Hydroxy-2-methylphenyl)propanoate | HCID 13551833 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 3-[4-(4-Bromo-phenoxy)-2-methyl-phenyl]-propionic acid methyl ester | HCID 57894135 | 42% |
Reaction Steps
A mixture of 3-(4-hydroxy-2-methyl-phenyl)-propionic acid methyl ester (2.0 g, 10.3 mmol), 1-bromo-4-iodobenzene (8.74 g, 30.9 mmol), cesium carbonate (4.03 g, 12.4 mmol), copper (I) chloride (0.51 g, 5.15 mmol) and 2,2,6,6-tetramethyl-3,5-heptanedione (0.47 g, 2.55 mmol) in 1-methyl-2-pyrrolidinone (20 mL) is heated to 120° C. for 1 hour under N2. The reaction is cooled and quenched with 1 N HCl. The mixture is then diluted with Et2O and extracted with water. The organic layer is dried (Na2SO4), and the solvent is removed in vacuo to afford crude product that is absorbed on silica gel and purified by flash chromatography using 9/1 hexanes/ethyl acetate to afford 1.51 g (42%) of the title compound. Rf=0.35 (4/1 hexanes/EtOAc). 1H NMR (400 MHz, CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608639B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-2073325a0895498ba00005dbff04257d |
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| Source note | uspto-grants-2009_10 |
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