化工社化工社 化学情報印刷レポート · 研究参考用
p-Fluoronitrobenzene → 1-[2,4-Bis(methoxymethoxy)-6-(4-nitrophenoxy)phenyl]ethanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Fluoronitrobenzene | HCID 9590 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1-[2-Hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanone | HCID 10879697 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 1-[2,4-Bis(methoxymethoxy)-6-(4-nitrophenoxy)phenyl]ethanone | HCID 66759310 | 52% |
反応手順
To a stirred suspension of 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanone (78 g, 298 mmol) and K2CO3 (45.3 g, 328 mmol) in DMSO (500 mL) and water (40 ml) was added 4-nitro-1-fluorobenzene (46.3 g, 328 mmol, 1.1 eq). After stirring for 15 min. at room temperature, the resulting suspension was heated for 6 hours at 55° C. After cooling, the dark solution was diluted with ethyl acetate (2000 mL) and thoroughly washed with 10% citric acid solution, then with brine and dried over Na2SO4. The solvent was removed and the residue was columned over silica gel eluting with cyclohexane/ethyl acetate 3/1, to provide the title compound (56 g, 52% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08993556B2 |
| 出典データセット | uspto-grants-2015_03 |
| ORD ID | ord-e370b93d25df41e0848e26659099a52e |
| 出典メモ | uspto-grants-2015_03 |