## Abstract As the second part of a series of studies on the synthesis of __n__‐butyl phenyl ether (ROPh) by tri‐liquid‐phase catalysis, this work examines the factors affecting the reaction between __n__‐butyl bromide (RBr, organic substrate) and sodium phenolate (NaOPh, aqueous nucleophile) with
A preliminary evaluation of a continuous-flow reactor for liquid–liquid–solid phase-transfer catalyzed synthesis of n-butyl phenyl ether
✍ Scribed by Hsu-Chin Hsiao; Wei-Chi Li; Hung-Shan Weng
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2005
- Tongue
- English
- Weight
- 183 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0268-2575
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
This study evaluates the feasibility of using a continuous‐flow stirred vessel reactor (CFSVR) to synthesize n‐butyl phenyl ether (ROPh) from n‐butyl bromide (RBr) and sodium phenolate (NaOPh) by liquid–liquid–solid phase‐transfer catalysis (triphase catalysis). The factors affecting the preparation of triphase catalysts, the etherification reaction in a batch reactor, and the performance in a CFSVR were investigated. The kinetic study with a batch reactor indicated that when the initial concentration of NaOPh or RBr was high, the conversion of RBr would depend on the initial concentration of both RBr and NaOPh. The reaction can be represented by a pseudo‐first‐order kinetic model when the concentration of NaOPh is in proper excess to that of RBr, and the apparent activation energy is 87.8 kJ mol^−1^. When the etherification reaction was carried out in the CFSVR, the catalyst particles did not flow out of the reactor, even at a high agitation speed. The conversion of RBr in the CFSVR was, as predicted, lower than that in the batch reactor, but was higher than the theoretical value because the dispersed phase is not completely mixed. Copyright © 2004 Society of Chemical Industry
📜 SIMILAR VOLUMES