2015
DOI: 10.1039/c5cy00347d
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Microwave rehydrated Mg–Al-LDH as base catalyst for the acetalization of glycerol

Abstract: Acetalization of glycerol with aldehydes to form cyclic acetals is an industrially important reaction and is generally carried out using acid catalysts.

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Cited by 36 publications
(16 citation statements)
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“…Similar pattern with drastic decrease in conversion and improved selectivity by p ‐anisaldehyde has also been reported by others [43] . This reduced reactivity is due to the introduction of an electron donating group on para position on the aromatic ring [44] of the aldehyde rendering the electrophilic site [45] . This hypothesis is supported by higher conversion reported in glycerol acetalization with aromatic aldehyde substituted with electron withdrawal group [40,46,47] .…”
Section: Resultssupporting
confidence: 83%
See 1 more Smart Citation
“…Similar pattern with drastic decrease in conversion and improved selectivity by p ‐anisaldehyde has also been reported by others [43] . This reduced reactivity is due to the introduction of an electron donating group on para position on the aromatic ring [44] of the aldehyde rendering the electrophilic site [45] . This hypothesis is supported by higher conversion reported in glycerol acetalization with aromatic aldehyde substituted with electron withdrawal group [40,46,47] .…”
Section: Resultssupporting
confidence: 83%
“…[43] This reduced reactivity is due to the introduction of an electron donating group on para position on the aromatic ring [44] of the aldehyde rendering the electrophilic site. [45] This hypothesis is supported by higher conversion reported in glycerol acetalization with aromatic aldehyde substituted with electron withdrawal group. [40,46,47] Thus, we showed here different types of substituents in aldehydes could affect the selectivity towards 1,3-dioxan-5-ol.…”
Section: Reusability Of A-46 In Acetalization Of Glycerol and Acetonementioning
confidence: 79%
“…The conversion of glycerol is negligible in the absence of a catalyst (Table 1, Entry 1), while it is significantly enhanced with ester sulfate-functionalized IL catalyst; for example, 73-86% of glycerol conversion and almost 97% acetal selectivity were demonstrated when ester sulfate-functionalized IL was used ( 4 ], 86% of glycerol was converted with 84% acetal yield, 28% of which consists of a six-membered compound, a versatile fine chemical, and an important intermediate in organic industrial chemistry. This six-membered product selectivity is higher than that found in many previous studies [5,14,16]. Generally, IL composes of an organic cation and an inorganic or organic anion, so it usually has a large structure than conventional homogeneous inorganic acidic catalysts (such as H 2 SO 4 and HCl).…”
Section: Introductioncontrasting
confidence: 41%
“…The intensity of the peak at 1420 cm -1 -attributed to carbonates -increased with the decrease in particle size, which figures a higher amount of adsorption sites for carbonate species on the samples with smaller crystallites The basicity of the catalysts was evaluated using temperature programmed CO 2 desorption (CO 2 -TPD) (Figure 3). The method is known to allow a quantitative analysis of basicity, with a distinction between weak, moderate and strong sites [26,27]. It should be noted, however, that a bulk gas/solid reaction may also occur during CO 2 adsorption, transforming sodium aluminate into sodium carbonate.…”
Section: Resultsmentioning
confidence: 98%