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HRID 127057生成日期:2026年10月23日

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 4-Benzoyloxy-1-octyne

https://huagongshe.com/zh-CN/reaction/127057

反应方程式

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-olHCID 103656—
溶剂吡啶HCID 1049—
产物4-Benzoyloxy-1-octyneHCID 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

DOI10.6084/m9.figshare.5104873.v1
专利号US04254285
来源数据集uspto-grants-1981_03
ORD IDord-e0fd92ab6e0248eeac81442cdf1319fc
来源说明uspto-grants-1981_03