V. V. Dotsenko, A. Z. Temerdashev, N. A. Aksenov, I. V. Aksenova, B. S. Krivokolysko, S. G. Krivokolysko
{"title":"伯硫酰胺与n -芳基-2-氯乙酰酰胺反应合成2,2′-硫比斯(n -芳基乙酰酰胺","authors":"V. V. Dotsenko, A. Z. Temerdashev, N. A. Aksenov, I. V. Aksenova, B. S. Krivokolysko, S. G. Krivokolysko","doi":"10.1134/S1070363225603655","DOIUrl":null,"url":null,"abstract":"<p>The reaction of thioacetamide, cyanothioacetamide, thiourea, 3-aryl-2-cyanothioacrylamides, (cyclohexylidene)cyanothioacetamide, or thiosemicarbazide with <i>N</i>-aryl-2-chloroacetamides in the presence of KOH in ethanol proceeds with the formation of the same products―2,2′-thiobis(<i>N</i>-arylacetamides)―in 62–93% yields. Structure of the products was confirmed by IR, NMR spectroscopy, and high-resolution mass spectrometry (HRMS).</p>","PeriodicalId":761,"journal":{"name":"Russian Journal of General Chemistry","volume":"95 9","pages":"2644 - 2652"},"PeriodicalIF":0.8000,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of 2,2′-Thiobis(N-arylacetamides) by Reaction of Primary Thioamides with N-Aryl-2-chloroacetamides\",\"authors\":\"V. V. Dotsenko, A. Z. Temerdashev, N. A. Aksenov, I. V. Aksenova, B. S. Krivokolysko, S. G. Krivokolysko\",\"doi\":\"10.1134/S1070363225603655\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The reaction of thioacetamide, cyanothioacetamide, thiourea, 3-aryl-2-cyanothioacrylamides, (cyclohexylidene)cyanothioacetamide, or thiosemicarbazide with <i>N</i>-aryl-2-chloroacetamides in the presence of KOH in ethanol proceeds with the formation of the same products―2,2′-thiobis(<i>N</i>-arylacetamides)―in 62–93% yields. Structure of the products was confirmed by IR, NMR spectroscopy, and high-resolution mass spectrometry (HRMS).</p>\",\"PeriodicalId\":761,\"journal\":{\"name\":\"Russian Journal of General Chemistry\",\"volume\":\"95 9\",\"pages\":\"2644 - 2652\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-10-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Journal of General Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1070363225603655\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of General Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1070363225603655","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Synthesis of 2,2′-Thiobis(N-arylacetamides) by Reaction of Primary Thioamides with N-Aryl-2-chloroacetamides
The reaction of thioacetamide, cyanothioacetamide, thiourea, 3-aryl-2-cyanothioacrylamides, (cyclohexylidene)cyanothioacetamide, or thiosemicarbazide with N-aryl-2-chloroacetamides in the presence of KOH in ethanol proceeds with the formation of the same products―2,2′-thiobis(N-arylacetamides)―in 62–93% yields. Structure of the products was confirmed by IR, NMR spectroscopy, and high-resolution mass spectrometry (HRMS).
期刊介绍:
Russian Journal of General Chemistry is a journal that covers many problems that are of general interest to the whole community of chemists. The journal is the successor to Russia’s first chemical journal, Zhurnal Russkogo Khimicheskogo Obshchestva (Journal of the Russian Chemical Society ) founded in 1869 to cover all aspects of chemistry. Now the journal is focused on the interdisciplinary areas of chemistry (organometallics, organometalloids, organoinorganic complexes, mechanochemistry, nanochemistry, etc.), new achievements and long-term results in the field. The journal publishes reviews, current scientific papers, letters to the editor, and discussion papers.