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聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 4-Benzoyloxy-1-octyne
参与物
| 角色 | 名称 | HCID | 投料 |
|---|---|---|---|
| 反应物 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 反应物 | 乙炔 | HCID 6326 | — |
| 反应物 | 苯甲酰氯 | HCID 7412 | — |
| 反应物 | 1-Octyn-4-ol | HCID 103656 | — |
| 溶剂 | 吡啶 | HCID 1049 | — |
| 产物 | 4-Benzoyloxy-1-octyne | HCID 20442054 | — |
反应步骤
To a stirred solution of 63. g (0.50 moles) of 1-octyn-4-ol (Example 93) in 500 ml of pyridine is added 77 g (0.55 moles) of benzoyl chloride. After stirring for 1.5 hours the mixture is treated with 10 ml of water, allowed to stand for 5 minutes, and concentrated. A solution of the residue in ether is washed successively with ice-cold hydrochloric acid, water, sodium bicarbonate solution, and brine. The solution is dried over magnesium sulfate, filtered through Celite, and concentrated to give an oil, λ max. 3240 (terminal acetylene) and 1730 cm-1 (benzyloxy group).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 专利号 | US04254285 |
| 来源数据集 | uspto-grants-1981_03 |
| ORD ID | ord-e0fd92ab6e0248eeac81442cdf1319fc |
| 来源说明 | uspto-grants-1981_03 |