-
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-Fluoro-3-pyridinemethanol is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products.
Due to its wide range of applications, there are several synthetic routes available for the synthesis of this compound.
In this article, we will discuss some of the most commonly used synthetic routes for the synthesis of 2-fluoro-3-pyridinemethanol.
- The classical route: The classical route for the synthesis of 2-fluoro-3-pyridinemethanol involves the reaction of 3-pyridinecarboxaldehyde with sodium fluoride in the presence of an acid catalyst.
The reaction results in the formation of 2-fluoro-3-pyridinemethanol, which can be isolated by precipitation with water. - The P2P (Phenyl-2-propan One-Pot) route: The P2P route is a one-pot synthesis route that involves the reaction of 2-phenyl-propionic acid with sodium fluoride in the presence of a solvent and a base catalyst.
The reaction results in the formation of 2-fluoro-3-pyridinemethanol, which can be isolated by filtration and washing with water. - The Boc method: The Boc method involves the protection of the hydroxyl group of 3-pyridinecarboxaldehyde with a tert-butyldimethylsilyl group using TBTU (O-(bis(tert-butyldimethylsilyl)oxy)) and DPC (1,8-diazabicyclo[5.
4.
0]undec-7-ene) in DMF (dimethylformamide) solvent.
After the reaction, the protecting group is removed with TFA (trifluoroacetic acid) in the presence of H2O (water) to obtain 2-fluoro-3-pyridinemethanol. - The oxidation method: The oxidation method involves the oxidation of 3-pyridinecarboxaldehyde with NaClO (sodium chlorite) in the presence of H2O2 (hydrogen peroxide) and a solvent.
The reaction results in the formation of 2-fluoro-3-pyridinemethanol, which can be isolated by filtration and washing with water. - The partial reduction method: The partial reduction method involves the reduction of 3-pyridinecarboxaldehyde with LiAlH4 (lithium aluminum hydride) in THF (tetrahydrofuran) solvent.
The reaction results in the formation of 2-fluoro-3-pyridinemethanol, which can be isolated by filtration and washing with water.
In conclusion, there are several synthetic routes available for the synthesis of 2-fluoro-3-pyridinemethanol.
The choice of route depends on various factors, such as the availability of reagents, the cost of the synthesis, and the desired yield.
The classical route and the P2P route are the most commonly used routes for the synthesis of this compound.
However, the Boc method, the oxidation method, and the partial reduction method are also useful for the synthesis of this compound and can be used in specific synthetic schemes.