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4-Fluoroiodobenzene → 1-(4-fluorophenyl)-3-(2-hydroxyethyl)-2(3H)-benzimidazolone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Fluoroiodobenzene | HCID 9605 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Iodide Ion | HCID 30165 | — |
| 反応物 | 1-(2-Hydroxyethyl)-1H-benzo[d]imidazol-2(3H)-one | HCID 4157423 | — |
| 触媒 | Zinc Oxide | HCID 3007857 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-(4-fluorophenyl)-3-(2-hydroxyethyl)-2(3H)-benzimidazolone | HCID 23282661 | 14.5% |
反応手順
A mixture of 1-(2-hydroxyethyl)benzimidazolone (J. Davoll, J. Chem. Soc., 1960, 308) (9 g), 4-fluoroiodobenzene (23 g), potassium carbonate (8.0 g), cupper(I) iodide (1 g), and zinc oxide (0.5 g) in N-methyl-2(3H)-pyrrolidinone (100 ml) was kept at 155° C. for 4.5 h. After cooling water (500 ml) was added followed by extraction with ethyl acetate (3×200 ml). The organic phase was washed with water and saturated calcium chloride solution and dried over magnesium sulfate. Removal of solvent in vacuo gave an oil which was purified by chromatography (silica gel, ethyl acetate) giving 1-(4-fluorophenyl)-3-(2-hydroxyethyl)-2(3H)-benzimidazolone (2 g) as a solid, mp: 124°-26° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05753661 |
| 出典データセット | uspto-grants-1998_05 |
| ORD ID | ord-a7520fd548084caeaa1dda9e18c00fe4 |
| 出典メモ | uspto-grants-1998_05 |