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Dimethylformamide → 4-(Diphenylmethyl)-1-piperazineethanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 1-(2-Hydroxyethyl)piperazine | HCID 7677 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Bromodiphenylmethane | HCID 236603 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-(Diphenylmethyl)-1-piperazineethanol | HCID 4742573 | 84.4% |
反応手順
To a mixture of 1-piperazineethanol (11.4 g), potassium carbonate powder (24.3 g) and N,N-dimethylformamide (100 ml) was added dropwise benzhydryl bromide (21.7 g). The mixture was stirred at room temperature for 2 hours, then diluted with water and extracted with ethyl ether. The ethyl ether layer was washed with saturated aquus sodium chloride and dried over sodium sulfate. The solvent was then distilled off and the residue was purified by silica gel chromatography [eluent: hexane-ethyl acetate (2:1)] to give 21.9 g (84.2%) of 4-benzhydryl-1-piperazineethanol as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04603135 |
| 出典データセット | uspto-grants-1986_07 |
| ORD ID | ord-a7f89949a20b48bfbffc559b3f3b5a68 |
| 出典メモ | uspto-grants-1986_07 |