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1,4-Dibromobutane → 7-(4-Bromobutoxy)-3-piperidino-2,2-dimethylbenzofuran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,4-Dibromobutane | HCID 8056 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 7-Hydroxy-3-piperidino-2,2-dimethylbenzofuran | HCID 14126650 | — |
| 触媒 | Tetrabutylammonium Chloride | HCID 70681 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 7-(4-Bromobutoxy)-3-piperidino-2,2-dimethylbenzofuran | HCID 21289001 | — |
反応手順
Crushed potassium hydroxide (19.6 g) and tetrabutyl ammonium chloride (1.7 g) are added to a solution of 7-hydroxy-3-piperidino-2,2-dimethylbenzofuran (14.4 g) in 1,4-dibromobutane (69.4 ml) and the mixture stirred at RT under nitrogen for 5 hours. The reaction mixture is diluted with ether, washed with water, extracted with 5% aq. HCl and the acidic phase washed with ether. The acidic phase is made basic thereby forming an oil which is taken up in ether, washed with sat'd aq. NaCl, dried, filtered and evaporated in vacuo affording the desired product as a liquid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04612309 |
| 出典データセット | uspto-grants-1986_09 |
| ORD ID | ord-931ac3f574254115bad1dfd8de4e47f9 |
| 出典メモ | uspto-grants-1986_09 |