-
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 synthesis of 2-chloro-3-methoxyquinoline, also known as 2C-M, is a complex process that involves several steps and various chemical reactions.
The chemical formula for 2C-M is C8H7ClNO, and it belongs to the class of substituted quinolines, a group of compounds that contain a quinoline backbone with one or more substitutions.
The synthesis of 2C-M can be achieved through several different routes, including the Williamson ether synthesis, the Grignard synthesis, and the Stickler reaction.
Each of these routes requires a different set of reagents and conditions, but they all involve the conversion of a starting material into the desired product.
The Williamson ether synthesis is a widely used method for the synthesis of 2C-M.
This route involves the condensation of an aldehyde or ketone with a halogenated alkyl or aryl ether, followed by reduction of the resulting intermediate to produce the desired quinoline.
The key step in this synthesis is the formation of the ether intermediate, which is typically prepared by the reaction of a Williamson base with a halogenated alkyl or aryl halide.
The Grignard synthesis is another common route for the synthesis of 2C-M.
This method involves the formation of a Grignard reagent, which is an organometallic compound that contains a carbon atom bonded to a magnesium atom.
The Grignard reagent is then treated with a halogenating reagent, such as a chloride or bromide, to produce the desired quinoline.
The Stickler reaction is a less commonly used route to 2C-M synthesis, but it involves a unique reaction mechanism that is based on the formation of a metal carbene complex.
In this synthesis, a benzaldehyde or benzene is treated with a reagent that contains a metal carbene ligand, such as titanium tetraisopropoxide, to form a carbene complex.
The carbene complex then undergoes a series of reactions to produce the desired quinoline.
Overall, the synthesis of 2C-M involves a complex series of chemical reactions that require careful selection of reagents and conditions.
Each of the synthetic routes has its own advantages and disadvantages, and the choice of route will depend on the availability of starting materials and the desired yield of the final product.
Nonetheless, the synthesis of 2C-M is an important step in the development of new chemical compounds for a variety of applications in the pharmaceutical and chemical industries.