-
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
The production process of 2-bromo-1-(2-fluoropyridin-3-yl)ethanone hydrobromide involves a series of chemical reactions that convert starting materials into the desired product.
The process can be broken down into several steps, each with its own specific chemical reaction and conditions.
Step 1: Synthesis of 2-fluoropyridine-3-carbaldehyde
The first step in the production process of 2-bromo-1-(2-fluoropyridin-3-yl)ethanone hydrobromide is the synthesis of 2-fluoropyridine-3-carbaldehyde.
This is achieved by reacting 2-fluoropyridine with acetaldehyde in the presence of a Lewis acid catalyst, such as aluminum chloride.
The reaction is carried out under inert gas conditions and at a temperature of around 80-100°C.
Step 2: Condensation of 2-fluoropyridine-3-carbaldehyde with acetone
The next step is the condensation of 2-fluoropyridine-3-carbaldehyde with acetone in the presence of a base, such as sodium hydroxide.
This reaction is carried out in a polar solvent, such as water, and at a temperature of around 50-60°C.
The product of this reaction is 2-fluoropyridin-3-yl acetate.
Step 3: Hydrolysis of 2-fluoropyridin-3-yl acetate
In the third step, 2-fluoropyridin-3-yl acetate is hydrolyzed using hydrochloric acid.
The reaction is carried out in a polar solvent, such as water, and at a temperature of around 20-30°C.
The product of this reaction is 2-fluoropyridin-3-ol.
Step 4: Bromination of 2-fluoropyridin-3-ol
In the fourth step, 2-fluoropyridin-3-ol is brominated using a bromine source, such as N-bromosuccinimide (NBS), in the presence of a Lewis acid catalyst, such as zinc chloride.
The reaction is carried out in a polar solvent, such as water, and at a temperature of around 0-10°C.
The product of this reaction is 2-bromo-1-(2-fluoropyridin-3-yl)ethanone.
Step 5: Hydrolysis of 2-bromo-1-(2-fluoropyridin-3-yl)ethanone
In the final step, 2-bromo-1-(2-fluoropyridin-3-yl)ethanone is hydrolyzed using hydrochloric acid, yielding the desired product, 2-bromo-1-(2-fluoropyridin-3-yl)ethanone hydrobromide.
Overall, the production process of 2-bromo-1-(2-fluoropyridin-3-yl)ethanone hydrobromide involves a series of chemical reactions that convert starting materials into the desired product.
The process requires the use of various chemical reagents, solvents, and catalysts, and must be carried out under specific conditions to ensure the desired product is obtained.
The process also requires the use of various equipment, such as reactors, condensers, and distillation columns, to separate and purify the product.
In conclusion, the production process of 2-bromo-1-(2-fluoropyridin-3-yl)ethanone hydrobromide is a multi-step process that requires careful attention to detail and the use of specialized equipment and chemicals.
The process involves