90322-32-0,With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.90322-32-0,2-Methylbenzo[d]oxazole-5-carboxylic acid,as a common compound, the synthetic route is as follows.
Step 2 – Preparation of Intermediate H 5-Carboxy-2-methylbenzoxazole (8.9 g) and methyl- p -toluenesulfonate (11.16 g) were combined and heated to 200C with stirring for 10 minutes. The mixture became a brown liquid and mild boiling occured. The reaction was cooled to room temperature and the liquid solidified. Acetone (50 ml) was added, and with constant heating at reflux, the product was broken up with a spatula. The resulting slurry was heated at reflux for 15 minutes with rapid stirring and the off-white product was collected by filtration. This product was slurried again in refluxing acetone for 30 minutes, filtered, washed with ligroin P950, and dried to yield 9.3 g of 5-carboxy-2,3-dimethylbenzoxazolium p -toluenesulfonate (Intermediate H).
The synthetic route of 90322-32-0 has been constantly updated, and we look forward to future research findings.
Reference£º
Patent; EASTMAN KODAK COMPANY, (a New Jersey corporation); EP294461; (1991); B1;,
Benzoxazole – Wikipedia
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