用過勞森試劑的小伙伴一定印象深刻，一方面被其難聞的氣味“勸退”，另一方面被其副產(chǎn)物難以除去而困擾，經(jīng)常和產(chǎn)物極性接近，過柱子又很容易拖尾，真是欲哭無淚啊。難聞的氣味咱可以忍忍，但純化困難是真的忍不了?。e急，小編在瀏覽文獻(xiàn)發(fā)現(xiàn)一篇文章分享了他們使用乙二醇和水加熱攪一攪然后分液的方法，成功除去了勞森試劑反應(yīng)后的副產(chǎn)物，無需過柱子，Wonderful!

下面讓我們一起看看這篇文章：

文章首先分析了勞森試劑發(fā)生硫代反應(yīng)后的副產(chǎn)物A，副產(chǎn)物A的極性常常和硫代產(chǎn)物極性接近，分離困難。

有文獻(xiàn)報(bào)道用碳酸氫鈉溶液可以將副產(chǎn)物A轉(zhuǎn)化為水溶性的B,進(jìn)而通過萃取除去雜質(zhì)( 這個(gè)方法小編試過，對(duì)小編的硫代酰胺反應(yīng)無效 )，然而這種方法會(huì)產(chǎn)生大量含磷廢水。

而本文作者將乙二醇和水加入勞森試劑硫代反應(yīng)后( 甲苯為溶劑 )的體系，加熱將副產(chǎn)物A轉(zhuǎn)化為大極性的C2( C2含有兩個(gè)羥基 )，分液后C2在乙二醇相，硫代產(chǎn)物在甲苯相，輕松完成副產(chǎn)物的分離，大功告成。( 小編親測(cè)有效，兩相都點(diǎn)過板，分的很干凈 ）

詳細(xì)步驟如下，他們還通過后續(xù)的重結(jié)晶，除色等操作完成了40 g規(guī)模的純化。

To a 500 mL three-necked flask 40.1 g of N2,N6-bis(2,4,6-trimethylphenyl)pyridine-2,6-(carbothioamide)(5, 0.10 mol), 41.2 g of Lawesson’s reagent(0.051 mol), and 200 mL of toluene were added. The mixture was heated to reflux under a nitrogen atmosphere. TLC monitoring showed that there still existed some amide-thioamide intermediate after 5 h and heating was continued for another 3 h. Afterwards, TLC monitoring showed that the amide-thioamide had nearly disappeared. Then, to the cooled mixture, were added 100 mL of ethylene glycol (excess), together with 1.0 mL of water and the resulting mixture was stirred at 95 °C. TLC monitoring of the toluene layer showed that the byproduct A of the Lawesson’s reagent had disappeared after 7.5 h. The slightly cooled mixture was transferred to a separation funnel. The toluene layer was separated, and the ethylene glycol layer and 50 mL of toluene were transferred back to the flask and stirred at 95 °C (oil bath) for 30 min. The toluene layers were combined, part of the solvent removed under reduced pressure and the remaining solution was heated to reflux and diluted with 100 mL of heptane. The solution remained clear during reflux. Then, the solution was cooled to precipitate the crystalline solid that was collected by filtration and washed with heptane (100 mL). Then, the solid was treated with 200 mL of toluene and 5.0 g of activated carbon at 80 °C, followed by hot filtration. The filtrate was concentrated to afford 39.5 g of the desired dithioamide 6 (91%) as bright yellow crystalline solid.

原文出處

Beilstein J. Org. Chem. 2021, 17, 805–812.