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HRID 654134作成日:2026年10月26日

Sodium ethoxide → Chlorfenapyr

https://huagongshe.com/reaction/654134

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ethoxideHCID 2723922—
反応物4-Bromo-1-(chloromethyl)-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carbonitrileHCID 19888616—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物ChlorfenapyrHCID 9177885.9%

反応手順

A solution of 4-bromo-1-(chloromethyl)-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carbonitrile (2.0 g, 0.005 mol) in absolute ethanol is treated with a 21% wt/wt ethanolic solution of sodium ethoxide (0.36 g, 0.0053 mol), heated to 75°-80° C. for 20-30 minutes, cooled to room temperature and diluted with water and ether. The organic phase is dried over anhydrous magnesium sulfate and concentrated in vacuo to give a solid which is recrystallized form heptane to give the title product as a white solid (1.75 g, mp 97°-98° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05130328
出典データセットuspto-grants-1992_07
ORD IDord-d87701a3380848998d4943e36ed4b71b
出典メモuspto-grants-1992_07