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1,3-Dibromopropane → 6-(3-Bromopropoxy)-4-piperidino-2,3-dihydrobenzopyran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,3-Dibromopropane | HCID 8001 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 6-Hydroxy-4-piperidino-2,3-dihydrobenzopyran | HCID 13712848 | — |
| 触媒 | Tetrabutylammonium Chloride | HCID 70681 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 6-(3-Bromopropoxy)-4-piperidino-2,3-dihydrobenzopyran | HCID 13712849 | — |
反応手順
Crushed potassium hydroxide (1.15 g) and tetrabutyl ammonium chloride (0.61 g) are added to a solution of the product obtained in Step 3. (4.8 g) in 1,3-dibromopropane (21 ml). The reaction mixture is stirred under nitrogen at RT for 48 hours, diluted with diethyl ether, washed with water and extracted into 5% aq. HCl. The aqueous solution is washed with ether and made alkaline yielding a yellow oil which is taken up in ether, washed, dried, filtered and evaporated to give the desired product as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04722925 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-000cebf4787344f1bf7d418a9168b1b4 |
| 出典メモ | uspto-grants-1988_02 |