-
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-5-fluoropyridine-4-boronic acid is a compound that has found use in various applications in the chemical industry.
Its synthetic routes have been extensively studied, and several methods have been developed to synthesize this compound.
This article will discuss some of the most popular synthetic routes for 2-bromo-5-fluoropyridine-4-boronic acid.
One of the earliest methods for synthesizing 2-bromo-5-fluoropyridine-4-boronic acid involved the use of borane-based reagents.
This method involved the reduction of 5-fluoro-2-nitro-pyridine-3-boronic acid with borane reagents in the presence of a base, such as sodium hydroxide.
The resulting compound was then treated with bromine to introduce the bromine atom.
This method was found to be effective, but it was also found to be somewhat tedious, as it required several steps to synthesize the final product.
A more efficient method for synthesizing 2-bromo-5-fluoropyridine-4-boronic acid involves the use of Pd(II) catalysts.
This method involves the reduction of 5-fluoro-2-chloropyridine-3-boronic acid with a Pd(II) catalyst in the presence of a reducing agent, such as hydrogen gas.
The resulting compound was then treated with bromine to introduce the bromine atom.
This method was found to be more efficient than the previous method, as it required fewer steps to synthesize the final product.
Another method for synthesizing 2-bromo-5-fluoropyridine-4-boronic acid involves the use of acid-base reactions.
This method involves the treatment of 5-fluoro-2-chloro-pyridine-3-boronic acid with a base, such as sodium hydroxide, to generate the boronic acid derivative.
The resulting compound was then treated with bromine and a Pd(II) catalyst to introduce the bromine atom.
This method was found to be efficient and cost-effective, as it allowed for the synthesis of the final product in a single step.
In recent years, other methods for synthesizing 2-bromo-5-fluoropyridine-4-boronic acid have been developed, such as the use of microwave irradiation and ultrasonication.
These methods have been found to be more efficient than traditional methods and have been widely adopted in the chemical industry.
Overall, the synthetic routes for 2-bromo-5-fluoropyridine-4-boronic acid have been extensively studied, and various methods have been developed to synthesize this compound.
These methods have been found to be effective and efficient, and have found widespread use in the chemical industry.
The development of new and more efficient synthetic routes for this compound is an ongoing process, and it is expected that even more efficient methods will be developed in the future.