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第 35 卷第 2 期Vol. 35 No. 2
2005 年 4 月Apr 2005

所屬欄目:其它

除草劑炔草酯的合成研究
陳強; 廖文文; 劉智凌(江蘇寶靈化工股份有限公司; 湖南師范大學(xué)化學(xué)化工學(xué)院; 湖南化工研究院; 江蘇南通; 湖南長(cháng)沙)
摘 要:以5氯2,3二氟吡啶與(R)2(對羥基苯氧基)丙酸為原料,以二甲基甲酰胺(DMF)為溶劑,K2CO3為縛酸劑,在70℃下醚化反應4h,然后再加入氯丙炔,以甲苯為溶劑,反應溫度70~75℃,降溫后過(guò)濾除鹽,DMF洗滌,脫溶,再用乙醇/水結晶,干燥得產(chǎn)品,含量98%,以(R)2(對羥基苯氧基)丙酸計總收率86%。
關(guān)鍵詞:炔草酯; 頂尖; 除草劑; 5-氯-2; 3-二氟吡啶; R-2-(對羥基苯氧基)丙酸
中圖分類(lèi)號:TQ457.2  文獻標識碼:A  文章編號:1009-9212(2005)02-0035-02
Synthesis of the herbcidal chodinafop-propargyl
CHEN Jing~(1); LIAO Wen-wen~(2)(1.Jiangsu Baoling Chemical Co Ltd; Nantong 226006; China; 2.Hunan Normal University; Changsha 410082; 3.Hunan Research Institute of Chemical Industry; Changsha 410007; China)
Abstract:Chodinafop-propargyl was synthesized from R-2-(p-hydroxyphenoxy)-propionic acid and 5-chloro 2,3-difluoropyridine and propargyl chloride. At first R-2-(p-hydroxyphenoxy)-propionic acid was converted into the corresonding potassium with potassium carbonate powder and tetrabutyl ammonium bromide in DMF at 70℃,then 5-chloro–2,3-difluoropyridine was added over course of 30 min ,after 4 hours, propargyl chloride was added over 2 hours to form the (R)(+)-2-[4-(5-chloro-3-fluoropyridin-2-yloxy)-phenoxy]-propionic ...
Key words:chodinafop-propargyl; Topic; herbcidal; l; 5-chloro–2; 3-difluoropyridine; R-2-(p-hydroxyphenoxy)-propionic acid
收稿日期:2004-02-26
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