{"id":1852,"date":"2021-02-23T05:20:12","date_gmt":"2021-02-22T21:20:12","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=1852"},"modified":"2021-02-23T05:20:12","modified_gmt":"2021-02-22T21:20:12","slug":"simple-exploration-of-5932-34-3","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=1852","title":{"rendered":"Simple exploration of 5932-34-3"},"content":{"rendered":"<p>Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 5932-34-3, name is Ethyl 4-bromo-1H-pyrazole-3-carboxylate, This compound has unique chemical properties. The synthetic route is as follows., <a href=\"https:\/\/www.ambeed.com\/products\/5932-34-3.html\">Application In Synthesis of  Ethyl 4-bromo-1H-pyrazole-3-carboxylate<\/a><\/p>\n<p>A) ethyl 4-bromo-1-(2,6-difluorobenzyl)-1H-pyrazole-3-carboxylate A solution of ethyl 4-bromo-1H-pyrazole-3-carboxylate (2.07 g) in THF (10 mL) was added to a solution of sodium hydride (60%, 0.454 g) in THF (10 mL) at 0C, and the mixture was stirred at 0C for 5 min. To the reaction mixture was added dropwise 2-(bromomethyl)-1,3-difluorobenzene (2.152 g) at 0C, and the mixture was gradually warmed to room temperature, and stirred overnight at room temperature. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate\/hexane) to give the title compound (3.16 g). MS: [M+H]+ 345.1.<\/p>\n<p>According to the analysis of related databases, 5932-34-3, the application of this compound in the production field has become more and more popular.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>According to the analysis of related databases, 5932-34-3, the application of this compound in the production field has become more and more popular.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[381,131],"tags":[127],"class_list":["post-1852","post","type-post","status-publish","format-standard","hentry","category-5932-34-3","category-pyrazoles-derivatives","tag-m-w200-300"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Simple exploration of 5932-34-3<\/title>\n<meta name=\"description\" content=\"Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 5932-34-3, name is Ethyl 4-bromo-1H-pyrazole-3-carboxylate, This compound has unique chemical properties. 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The synthetic route is as follows., Application In Synthesis of Ethyl 4-bromo-1H-pyrazole-3-carboxylate","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":"http:\/\/www.pyrazoles-derivatives.com\/?p=1852","og_locale":"en_US","og_type":"article","og_title":"Simple exploration of 5932-34-3","og_description":"Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 5932-34-3, name is Ethyl 4-bromo-1H-pyrazole-3-carboxylate, This compound has unique chemical properties. 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