Kinetics for benzoylation of sodium 4-acetylphenoxide via third-liquid phase in the phase-transfer catalysis
In this research, the kinetics for synthesizing 4-acetylphenyl benzoate (R *COOR) from benzoylation of sodium 4-acetylphenoxide via third-liquid phase-transfer catalysis was investigated. The reaction rate was observed to be strongly dependent on agitation speeds in the third-phase catalytic reactio...
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Veröffentlicht in: | Applied catalysis. A, General General, 2005-08, Vol.290 (1), p.65-72 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this research, the kinetics for synthesizing 4-acetylphenyl benzoate (R
*COOR) from benzoylation of sodium 4-acetylphenoxide via third-liquid phase-transfer catalysis was investigated. The reaction rate was observed to be strongly dependent on agitation speeds in the third-phase catalytic reaction. By forming the third-liquid phase, the observed reaction can be greatly enhanced to give a product yield of 100% in a duration of 3
min at 20
°C and 200
rpm. If a third-liquid phase was not formed in the liquid–liquid system, the reaction rate is very slow and the product yield is only 2% in 3
min at 20
°C. The reaction conducted in third-liquid phase-transfer catalytic system is faster than that in LLPTC system by 25–28 times. The amount of catalytic intermediate (QOR) in the third-liquid phase was about 50% of the catalyst initially added and kept about 30% of it remained after 1
min, and only small amounts of a catalytic intermediate residing in the organic phase were observed during the reaction using methyl
t-butyl ether as the solvent. The concentration of catalytic intermediate slightly decreased with increasing reaction time, while the molar ratio of QOR to benzyl tri-
n-butylammonium cation in the third-liquid phase remained almost constant after 1
min and increased with increasing agitation speeds. The experimental results were well described by the pseudo-first-order kinetics. The present work shows an effective method to synthesize 4-acetylphenyl benzoate. |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2005.05.014 |