{"id":1176,"date":"2020-12-03T15:30:35","date_gmt":"2020-12-03T07:30:35","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=1176"},"modified":"2020-12-03T15:30:35","modified_gmt":"2020-12-03T07:30:35","slug":"new-downstream-synthetic-route-of-3-difluoromethyl-1-methyl-1h-pyrazole-4-carboxylic-acid","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=1176","title":{"rendered":"New downstream synthetic route of  3-(Difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid"},"content":{"rendered":"<p><a href=\"https:\/\/www.ambeed.com\/products\/176969-34-9.html\">176969-34-9<\/a>, Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 176969-34-9, name is 3-(Difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid, A new synthetic method of this compound is introduced below.<\/p>\n<p>The pyrazole acid chloride is prepared from 3- difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid and thionyl chloride in heptane shortly before use. In a 500-mL round-bottomed flask provided with alkaline scrubber, pyrazole acid (74.0 grams, 0.42 mol) is suspended in heptane (170 mL) . Dimethylformamide (0.70 grams, 0.009 mol) and thionyl chloride (55.0 grams, 0.462 mol) are added and the bi-phasic mixture is stirred and heated at 42-45 C.After complete conversion of pyrazole acid (2.5 hours), the solvent and excess thionyl chloride are completely removed by vacuum distillation.Liquid pyrazole acid chloride is obtained as the residue (approximately 81.0 grams)<\/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":[173,131],"tags":[126],"class_list":["post-1176","post","type-post","status-publish","format-standard","hentry","category-176969-34-9","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 downstream synthetic route of 3-(Difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid<\/title>\n<meta name=\"description\" content=\"176969-34-9, Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. 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