{"title":"1,1,1,3,3,3-六氟-2-丙醇可重复使用介质:绿色无催化剂合成吡喃[2,3-d]嘧啶支架","authors":"Farzaneh Mohamadpour","doi":"10.1007/s12039-024-02334-x","DOIUrl":null,"url":null,"abstract":"<div><p>A safe method of producing pyrano[2,3-<i>d</i>]pyrimidine scaffolds without the need for a catalyst is shown, utilizing the concepts of green chemistry. This is achieved by employing polyfluorinated alcohol as a reusable medium and mixing barbituric acid/1,3-dimethylbarbituric acid, malononitrile and aryl aldehydes in an environmentally friendly manner. This environmentally friendly method uses one pot, readily accessible, low-cost reaction media, safe reaction conditions, no requirement for column chromatography for separation and effective use of resources. Furthermore, green 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) did not require significant modifications and remained stable for four reuses. This is highly helpful in satisfying industrial demands and resolving environmental issues.</p><h3>Graphical abstract</h3><p>Our study shows that 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) is used as a reusable medium to synthesize pyrano[2,3-<i>d</i>]pyrimidine frameworks without the need for a catalyst. This eco-friendly, cost-effective and straightforward solution has several benefits. It employs readily accessible materials, reduces the need for costly and dangerous chemicals, saves time and yields high-quality results.\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":616,"journal":{"name":"Journal of Chemical Sciences","volume":"137 1","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2024-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"1,1,1,3,3,3-hexafluoro-2-propanol as a reusable media: Green and catalyst-free synthesis of pyrano[2,3-d]pyrimidine scaffolds\",\"authors\":\"Farzaneh Mohamadpour\",\"doi\":\"10.1007/s12039-024-02334-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A safe method of producing pyrano[2,3-<i>d</i>]pyrimidine scaffolds without the need for a catalyst is shown, utilizing the concepts of green chemistry. This is achieved by employing polyfluorinated alcohol as a reusable medium and mixing barbituric acid/1,3-dimethylbarbituric acid, malononitrile and aryl aldehydes in an environmentally friendly manner. This environmentally friendly method uses one pot, readily accessible, low-cost reaction media, safe reaction conditions, no requirement for column chromatography for separation and effective use of resources. Furthermore, green 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) did not require significant modifications and remained stable for four reuses. This is highly helpful in satisfying industrial demands and resolving environmental issues.</p><h3>Graphical abstract</h3><p>Our study shows that 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) is used as a reusable medium to synthesize pyrano[2,3-<i>d</i>]pyrimidine frameworks without the need for a catalyst. This eco-friendly, cost-effective and straightforward solution has several benefits. It employs readily accessible materials, reduces the need for costly and dangerous chemicals, saves time and yields high-quality results.\\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":616,\"journal\":{\"name\":\"Journal of Chemical Sciences\",\"volume\":\"137 1\",\"pages\":\"\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-12-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Sciences\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s12039-024-02334-x\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-024-02334-x","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
1,1,1,3,3,3-hexafluoro-2-propanol as a reusable media: Green and catalyst-free synthesis of pyrano[2,3-d]pyrimidine scaffolds
A safe method of producing pyrano[2,3-d]pyrimidine scaffolds without the need for a catalyst is shown, utilizing the concepts of green chemistry. This is achieved by employing polyfluorinated alcohol as a reusable medium and mixing barbituric acid/1,3-dimethylbarbituric acid, malononitrile and aryl aldehydes in an environmentally friendly manner. This environmentally friendly method uses one pot, readily accessible, low-cost reaction media, safe reaction conditions, no requirement for column chromatography for separation and effective use of resources. Furthermore, green 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) did not require significant modifications and remained stable for four reuses. This is highly helpful in satisfying industrial demands and resolving environmental issues.
Graphical abstract
Our study shows that 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) is used as a reusable medium to synthesize pyrano[2,3-d]pyrimidine frameworks without the need for a catalyst. This eco-friendly, cost-effective and straightforward solution has several benefits. It employs readily accessible materials, reduces the need for costly and dangerous chemicals, saves time and yields high-quality results.
期刊介绍:
Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.