首页> 外文期刊>Tetrahedron >An eco-friendly protocol for synthesis of thiourea derivatives: 1-benzoyl-3-benzylguanidine and 1-benzoyl-3-benzyl-O-ethylisourea. A possible non-purely thermal microwave assisted reaction
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An eco-friendly protocol for synthesis of thiourea derivatives: 1-benzoyl-3-benzylguanidine and 1-benzoyl-3-benzyl-O-ethylisourea. A possible non-purely thermal microwave assisted reaction

机译:合成硫脲衍生物的生态友好方案:1-苯甲酰基-3-苄基胍和1-苯甲酰基-3-苄基-O-乙基异脲。可能的非纯热微波辅助反应

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摘要

1-Benzoyl-3-benzylguanidine and 1-benzoyl-3-benzyl-O-ethylisourea were synthesized in good yields (68 and 76%, respectively) from 1-benzoyl-3-benzylthiourea and benzoyl-ethylthiocarbamate in dry media conditions using KF-Al2O3 under microwave irradiation. Strong nucleophilic amines promoted the sulfur elimination by attack on the thiocarbonyl group in both thiourea and thiocarbamates to afford guanidines and isourea, respectively. Transesterification products were obtained from p-TsOH catalyzed reaction of thiocarbamate with alcohols under MW-solvent-free conditions. Very important non-purely thermal MW specific effects were evidenced and attributed to stabilization by coulombic interactions between materials and waves. (c) 2005 Elsevier Ltd. All rights reserved.
机译:使用KF在干燥介质条件下从1-苯甲酰基-3-苄基硫脲和苯甲酰基-乙基硫代氨基甲酸酯以良好的收率(分别为68%和76%)合成了1-苯甲酰基-3-苄基胍和1-苯甲酰基-3-苄基-O-乙基异脲-Al2O3在微波辐射下。强亲核胺通过攻击硫脲和硫代氨基甲酸酯中的硫代羰基而促进了硫的消除,从而分别提供了胍和异脲。在无MW溶剂的条件下,由p-TsOH催化的硫代氨基甲酸酯与醇的反应获得酯交换产物。证明了非常重要的非纯热MW特有效应,并归因于物质与波浪之间的库仑相互作用而稳定。 (c)2005 Elsevier Ltd.保留所有权利。

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