-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
-
Cosmetic Ingredient
- Water Treatment Chemical
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
2-Bromo-1,3,4-thiadiazole is a versatile organic compound that has found numerous applications in various fields such as medicinal chemistry, materials science, and electrochemistry.
The synthetic routes for this compound have been extensively studied, and several methods have been developed over the years.
In this article, we will discuss some of the most common synthetic routes for 2-bromo-1,3,4-thiadiazole.
One of the most straightforward methods for synthesizing 2-bromo-1,3,4-thiadiazole involves the reaction of thiourea with bromine in the presence of a solvent such as water or ethanol.
This reaction results in the formation of the thiadiazole derivative, which can then be hydrolyzed to obtain the desired product.
Another synthetic route involves the reduction of 2-nitro-1,3,4-thiadiazole using a reducing agent such as hydride or lithium aluminum hydride (LiAlH4).
This reaction results in the formation of 2-bromo-1,3,4-thiadiazole.
Another synthetic route involves the reaction of 1,3,4-thiadiazole-2-thiol with bromine in the presence of a solvent such as carbon tetrachloride or chloroform.
This reaction results in the formation of 2-bromo-1,3,4-thiadiazole.
Yet another synthetic route involves the reaction of 2-mercaptobenzimidazole with bromine in the presence of a solvent such as ether or benzene.
This reaction results in the formation of 2-bromo-1,3,4-thiadiazole.
In addition to the above-mentioned synthetic routes, several other methods have also been reported in the literature for the synthesis of 2-bromo-1,3,4-thiadiazole.
These include the reduction of 2-bromothiophene-3-sulfonate with hydride, the reaction of thiuram monomer with bromine, and the reaction of 2-thiothiophene-3-carboxaldehyde with bromine in the presence of a Lewis acid catalyst.
Overall, the synthetic routes for 2-bromo-1,3,4-thiadiazole are varied and versatile, and several methods can be used depending on the specific requirements of the application.
The compound is widely used in various fields and its demand is expected to continue to grow in the future.
As a result, the development of new and efficient synthetic routes for 2-bromo-1,3,4-thiadiazole will continue to be an area of active research in the chemical industry.