1590352-67-2

Upstream product

• 1236568-49-2 5-iodo-2,2-dimethyl-4H-benzo[d][1,3]oxathiin-4-one 
• 67-56-1 methanol 
• 1236571-14-4 5-(furan-2-yl)-2,2-dimethyl-4H-benzo[d][1,3]oxathiin-4-one 
• 38058-01-4 2,2-dimethyl-4H-benzo[d][1,3]oxathiin-4-one 
• 147-93-3 Thiosalicylic acid 

Relevant academic research and scientific papers

Efficient synthesis of functionalized 6-substituted-thiosalicylates via microwave-promoted Suzuki cross-coupling reaction

Functionalized 6-substituted-thiosalicylates are key intermediates for the synthesis of pyrimidinyl(thio)salicylic acids, a group of important herbicides targeting plant acetohydroxyacid synthase. Therefore, it is of great interest to develop an efficient method for the syntheses of 6-substituted-thiosalicylates. Herein, we have developed a direct and efficient method for the synthesis of functionalized 6-substituted-thiosalicylates (4) from aryl iodide (1) by using an improved microwave-assisted Suzuki cross-coupling reaction. Almost all the reactions proceeded smoothly and afforded moderate to excellent yields of products. Moreover, this protocol is obviously superior to the traditional available methods and could be utilized to synthesize pyrimidinyl(thio)salicylic acid and its derivatives.