Pentaethylphenol (Not 2,6-di-tert-butyl-4-ethylphenol) verified as the primary product of guaiacol ethanol alkylation reaction

IF 5.2 2区 化学 Q1 CHEMISTRY, APPLIED Catalysis Today Pub Date : 2024-09-26 DOI:10.1016/j.cattod.2024.115081
Yushuai Sang , Mingze Yang , Cedric Agyingi, Yongdan Li
{"title":"Pentaethylphenol (Not 2,6-di-tert-butyl-4-ethylphenol) verified as the primary product of guaiacol ethanol alkylation reaction","authors":"Yushuai Sang ,&nbsp;Mingze Yang ,&nbsp;Cedric Agyingi,&nbsp;Yongdan Li","doi":"10.1016/j.cattod.2024.115081","DOIUrl":null,"url":null,"abstract":"<div><div>Guaiacol ethanol alkylation (GEA), a model reaction of lignin solvolysis, has been intensively investigated. However, the product identification with gas chromatograph-mass spectrometer (GC-MS) was wrong due to the defect of the GC-MS databases. In this work, the main product was isolated with a flash chromatography technique and analyzed with <sup>1</sup>H NMR and was identified as ethyl fully substituted phenol (or pentaethylphenol), which is contrary to the reported 2,6-di-tert-butyl-4-ethylphenol in previous literature. The NMR analysis of the entire product mixture further confirms that the product only contains ethyl substituted molecules, with no existence of isopropyl or tert-butyl substituted products. The byproducts, including ethyl partially substituted phenols, i.e., tetraethylphenol and triethylphenol, ethyl partially substituted guaiacol, 2-ethoxyphenol, and pentaethylbenzene, were also speculated based on the MS spectra. These findings rectify a long-standing error in product identification and may offer critical insights for mechanism investigations.</div></div>","PeriodicalId":264,"journal":{"name":"Catalysis Today","volume":"445 ","pages":"Article 115081"},"PeriodicalIF":5.2000,"publicationDate":"2024-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Today","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920586124005753","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

Guaiacol ethanol alkylation (GEA), a model reaction of lignin solvolysis, has been intensively investigated. However, the product identification with gas chromatograph-mass spectrometer (GC-MS) was wrong due to the defect of the GC-MS databases. In this work, the main product was isolated with a flash chromatography technique and analyzed with 1H NMR and was identified as ethyl fully substituted phenol (or pentaethylphenol), which is contrary to the reported 2,6-di-tert-butyl-4-ethylphenol in previous literature. The NMR analysis of the entire product mixture further confirms that the product only contains ethyl substituted molecules, with no existence of isopropyl or tert-butyl substituted products. The byproducts, including ethyl partially substituted phenols, i.e., tetraethylphenol and triethylphenol, ethyl partially substituted guaiacol, 2-ethoxyphenol, and pentaethylbenzene, were also speculated based on the MS spectra. These findings rectify a long-standing error in product identification and may offer critical insights for mechanism investigations.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
经证实五乙基苯酚(不是 2,6-二叔丁基-4-乙基苯酚)是愈创木酚乙醇烷基化反应的主要产物
愈创木酚乙醇烷基化反应(GEA)是木质素溶解的一个模型反应,已被深入研究。然而,由于气相色谱-质谱(GC-MS)数据库的缺陷,用气相色谱-质谱(GC-MS)鉴定产物时出现了错误。在这项工作中,利用闪蒸色谱技术分离出了主要产物,并用 1H NMR 进行了分析,确定其为乙基全取代苯酚(或五乙基苯酚),这与之前文献中报道的 2,6-二叔丁基-4-乙基苯酚相反。对整个产品混合物的核磁共振分析进一步证实,该产品只含有乙基取代的分子,不存在异丙基或叔丁基取代的产品。根据质谱图还推测出了副产物,包括乙基部分取代的苯酚,即四乙基苯酚和三乙基苯酚、乙基部分取代的愈创木酚、2-乙氧基苯酚和五乙苯。这些发现纠正了产品鉴别中长期存在的错误,并可能为机理研究提供重要启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
期刊介绍: Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues. Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.
期刊最新文献
The peculiar role of copper in the saccharides hydrogenation in aqueous phase Editorial Board Establishing the oxygen evolution reaction pathway on iron-oxy-hydroxide through electro-kinetic study Sulfur-doped carbon/TiO2 composites for ethylene photo-oxidation. Enhanced performance by doping TiO2 phases with sulfur by mobile species inserted on the carbon support Tetravalent metals modulated Zn-based layered double hydroxides and their mixed metal oxides for catalytic depolymerization of carbonyl-coordinating plastic waste
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1