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One-pot synthesis of cyclic aldol tetramer and ?, β-unsaturated aldol from linear aldehydes using quaternary ammonium combined with sodium hydroxide as catalysts

One-pot synthesis of cyclic aldol tetramer and ?, β-unsaturated aldol from linear aldehydes using quaternary ammonium combined with sodium hydroxide as catalysts
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摘要 One-pot synthesis of cyclic aldol tetramer and α, β-unsaturated aldol from C3-C8 linear aldehydes using phase-transfer catalyst(PTC), quaternary ammonium, combined with sodium hydroxide as catalysts was investigated. Butanal was subjected for detail investigations to study the effect of parameters. It was found that the selectivity of cyclic aldol tetramer depends greatly on the operating conditions of the reaction, especially the PTC/butanal molar ratio. The average selectivity of 2-hydroxy-6-propyl-l, 3, 5-triethyl-3-cyclohexene-1-carboxaldehyde(HPTECHCA) was 54.41% using tetrabutylammonium chloride combined with 14%(mass fraction) Na OH as catalysts at 60 °C for 2 h with a PTC-to-butanal molar ratio of 0.09:1. Pentanal was more likely to generate cyclic aldol tetramer compared with other aldehydes under the optimum experimental conditions. Recovery of the PTC through water washing followed by adding enough sodium hydroxide from the washings was also demonstrated. One-pot synthesis of cyclic aldol tetramer and α, β-unsaturated aldol from C3-C8 linear aldehydes using phase-transfer catalyst(PTC), quaternary ammonium, combined with sodium hydroxide as catalysts was investigated. Butanal was subjected for detail investigations to study the effect of parameters. It was found that the selectivity of cyclic aldol tetramer depends greatly on the operating conditions of the reaction, especially the PTC/butanal molar ratio. The average selectivity of 2-hydroxy-6-propyl-l, 3, 5-triethyl-3-cyclohexene-1-carboxaldehyde(HPTECHCA) was 54.41% using tetrabutylammonium chloride combined with 14%(mass fraction) Na OH as catalysts at 60 ℃for 2 h with a PTC-to-butanal molar ratio of 0.09:1. Pentanal was more likely to generate cyclic aldol tetramer compared with other aldehydes under the optimum experimental conditions. Recovery of the PTC through water washing followed by adding enough sodium hydroxide from the washings was also demonstrated.
出处 《Journal of Central South University》 SCIE EI CAS CSCD 2015年第6期2081-2087,共7页 中南大学学报(英文版)
基金 Project(2013AA064102)supported by the National High-Tech Research Program of China Project(11JJ6014)supported by the Hunan Provincial Natural Science Foundation of China
关键词 相转移催化剂 不饱和醛 一锅法合成 氢氧化钠 环缩合 季铵盐 线性 最佳实验条件 aldol condensation one-pot synthesis phase-transfer catalyst aldehyde
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