Analyzing the synthesis route of 2382-96-9

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Benzo[d]oxazole-2-thiol, 2382-96-9

2382-96-9, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Benzo[d]oxazole-2-thiol, cas is 2382-96-9,the benzoxazole compound, it is a common compound, a new synthetic route is introduced below.

General procedure: A mixture of thiol (1 mmol), H2O2 (0.4 mL) and catalyst(0.01 g) was stirred in ethanol at room temperature for thecertain period of time. The reaction was monitored byTLC. After completion of the reaction, the catalyst wasseparated by simple filtration and the mixture was washedwith CH2Cl2 (5 9 2 mL), and next, the product wasextracted with CH2Cl2 (5 mL 9 4). The organic layer wasdried over anhydrous Na2SO4 (1.5 g). After the evaporationof dicoloromethan gave the pure products in 85-98 %yields.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Benzo[d]oxazole-2-thiol, 2382-96-9

Reference:
Article; Hajjami, Maryam; Yousofvand, Zakieh; Catalysis Letters; vol. 145; 9; (2015); p. 1733 – 1740;,
Benzoxazole – Wikipedia
Benzoxazole | C7H5NO – PubChem