HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465559Generated: November 1, 2026
Cesium carbonate → 1-{4-((5-Methoxypyridin-2-yl)oxy)-2,6-dimethylphenyl}ethanone
https://huagongshe.com/reaction/1465559
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | N,N-Dimethylglycine hydrochloride | HCID 75605 | — |
| Reactant | 1-(4-Hydroxy-2,6-dimethylphenyl)ethanone | HCID 4057370 | — |
| Reactant | 2-Bromo-5-methoxypyridine | HCID 11148151 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-{4-((5-Methoxypyridin-2-yl)oxy)-2,6-dimethylphenyl}ethanone | HCID 86690862 | 107% |
Reaction Steps
A mixture of 2-bromo-5-methoxypyridine (18-1, 1.03 g, 5.46 mmol), 1-(4-hydroxy-2,6-dimethylphenyl)ethanone (4-2, 0.80 g, 4.89 mmol), N,N-dimethylglycine HCl salt (0.28 g, 1.95 mmol), copper iodide (0.24 g, 1.24 mmol), and cesium carbonate (3.57 g, 10.96 mmol) in dioxane (10 mL) was heated at 120° C. for 4.0 h. The reaction mixture was cooled to room temperature, added with water, and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous MgSO4, and concentrated to give 1-{4-((5-methoxypyridin-2-yl)oxy)-2,6-dimethylphenyl}ethanone (18-2, 1.42 g) as a yellow oil in 96% yield, which was used directly for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999983B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-213196f336134868a8f83dc613ba295c |
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| Source note | uspto-grants-2015_04 |
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