Facile and efficient acylation of chitin in deep eutectic solvents

Yusuke Egi, Jun-ichi Kadokawa
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引用次数: 1

Abstract

This study investigates acylation of chitin in deep eutectic solvents (DESs) as analogous solvents of ionic liquids (ILs), because we have already reported that such reaction smoothly progresses using acyl chlorides in the presence of pyridine/N,N-dimethyl-4-aminopyridine (DMAP) as base/catalyst in the IL, that dissolves chitin. In addition to a DES composed of 1-allyl-3-methylimidazolium chloride (AMIMCl) and thiourea (TUA) as hydrogen bond acceptor and donor (HBA and HBD), respectively, which we previously reported to dissolve chitin, several DESs were prepared from AMIMCl and different HBDs, that is, urea (UA), acetylthiourea (AcTUA), acetylurea (AcUA), and 1,1,3,3-tetramethylguanidine (TMG). These DESs were found to also dissolve chitin. Hexanoylation of chitin in the AMIMCl/TUA-DES under the same conditions, as those previously performed in the IL, i.e., using hexanoyl chloride in the presence of pyridine/DMAP at 100 ​°C for 24 ​h, gave the product with the low degree of substitution (DS). As this was speculated to be due to the high nucleophilicity of TUA, which had a potential to react with hexanoyl chloride, the other HBDs with lower nucleophilicity, mentioned above, were employed to be combined with AMIMCl in the DESs. When hexanoylation of chitin was carried out in the DESs composed of UA, AcTUA, AcUA, and TMG under the same conditions as above, the higher DS products were obtained. In particular, the reaction in the AMIMCl/TMG-DES efficiently occurred in the absence of pyridine/DMAP to produce the high DS product, probably owing to the high basicity and low nucleophilicity of TMG. The structure of the chitin hexanoate produced was evaluated by the IR and 1H NMR measurements. Accordingly, acylation of chitin using various acyl chlorides was performed in the AMIMCl/TMG-DES under the conditions without the use of pyridine/DMAP to give the corresponding chitin acylates with the high DSs. This study achieves the facile and efficient acylation method of chitin in the DES.

Abstract Image

几丁质在深共晶溶剂中容易和有效的酰化
本研究研究了在深度共晶溶剂(DESs)中作为离子液体(ILs)的类似溶剂的甲壳质的酰化,因为我们已经报道了在吡啶/N,N-二甲基-4-氨基吡啶(DMAP)作为碱/催化剂的存在下,使用酰氯在离子液体中溶解甲壳质,这种反应顺利进行。除了由1-烯丙基-3-甲基氯化咪唑鎓(AMIMCl)和硫脲(TUA)分别作为氢键受体和供体(HBA和HBD)组成的DES(我们之前报道过它们可以溶解几丁质)之外,还由AMIMCl和不同的HBD制备了几种DES,即脲(UA)、乙酰硫脲(AcTUA)、乙酰脲(AcUA)和1,1,3,3-四甲基胍(TMG)。发现这些DESs也能溶解几丁质。在与先前在IL中进行的条件相同的条件下,即在吡啶/DMAP存在下,在100​°C 24​h、 得到具有低取代度(DS)的产物。由于这被推测是由于TUA的高亲核性,其具有与己酰氯反应的潜力,因此上述具有较低亲核性的其他HBD被用于在DESs中与AMIMCl组合。当在与上述相同的条件下在由UA、AcTUA、AcUA和TMG组成的DESs中进行甲壳质的己酰化时,获得更高的DS产物。特别地,AMIMCl/TMG-DES中的反应在不存在吡啶/DMAP的情况下有效地发生以产生高DS产物,这可能是由于TMG的高碱度和低亲核性。通过IR和1H NMR测量评估了制备的己酸甲壳质的结构。因此,在不使用吡啶/DMAP的条件下,在AMIMCl/TMG-DES中使用各种酰氯对甲壳质进行酰化,得到具有高DS的相应甲壳质酰化物。本研究实现了甲壳素在DES中的简单有效的酰化方法。
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