{"id":1525,"date":"2021-01-20T02:43:19","date_gmt":"2021-01-19T18:43:19","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=1525"},"modified":"2021-01-20T02:43:19","modified_gmt":"2021-01-19T18:43:19","slug":"new-learning-discoveries-about-180207-57-2","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=1525","title":{"rendered":"New learning discoveries about 180207-57-2"},"content":{"rendered":"<p>Adding a certain compound to certain chemical reactions, such as: 180207-57-2, name is 2-(1H-Pyrazol-4-yl)ethanol, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound  180207-57-2, <a href=\"https:\/\/www.ambeed.com\/products\/180207-57-2.html\">Quality Control of 2-(1H-Pyrazol-4-yl)ethanol<\/a><\/p>\n<p>A solution of 2-(1H-pyrazol-4-yl)ethan-1-ol (3.00 g, 26.75 mmol, 1.00 equiv), SEM-Cl (7.00 mL, 43.18 mmol, 1.61 equiv) and Cs2CO3 (13.00 g, 39.89 mmol, 1.49 equiv) in N,N-dimethylformamide (20 mL) was stirred for 3 h at room temperature. When LCMS indicated most of starting material was converted into the desired product, the resulting solution was concentrated and diluted with 150 mL of dichloromethane, washed with 3&#215;50 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by a silica gel column eluting with DCM\/MeOH (10:1) to afford 2.6 g of the title compound as yellow oil.<\/p>\n<p>If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[211,131],"tags":[126],"class_list":["post-1525","post","type-post","status-publish","format-standard","hentry","category-180207-57-2","category-pyrazoles-derivatives","tag-m-w100-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>New learning discoveries about 180207-57-2<\/title>\n<meta name=\"description\" content=\"Adding a certain compound to certain chemical reactions, such as: 180207-57-2, name is 2-(1H-Pyrazol-4-yl)ethanol, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. 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Here is a downstream synthesis route of the compound 180207-57-2, Quality Control of 2-(1H-Pyrazol-4-yl)ethanol","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.pyrazoles-derivatives.com\/?p=1525","og_locale":"en_US","og_type":"article","og_title":"New learning discoveries about 180207-57-2","og_description":"Adding a certain compound to certain chemical reactions, such as: 180207-57-2, name is 2-(1H-Pyrazol-4-yl)ethanol, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. 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