-
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 synthetic routes of 5-methylbenzo[b]thiophene are widely studied and utilized in the chemical industry due to its diverse range of applications.
This thiophene derivative is commonly found in various natural products, such as thymoquinone and sesquithymoquinone, and has been extensively researched for its potential as a pharmaceutical agent, antioxidant, and as a material for organic electronics.
One of the most common synthetic routes for 5-methylbenzo[b]thiophene is through the reaction of 2-methyl-5-butylthiophene-2-carboxaldehyde with sodium hydroxide in the presence of a Lewis acid catalyst, such as boron trifluoride.
This reaction results in the formation of 5-methylbenzo[b]thiophene, which can then be further oxidized to produce 5-methylbenzo[b]thiophene-2,2-dioxide.
Another commonly used route involves the condensation of 2-methyl-5-butylthiophene-2-carbaldehyde with benzaldehyde in the presence of a strong acid catalyst, such as sulfuric acid.
This reaction results in the formation of 5-methylbenzo[b]thiophene, which can be further converted to the desired product through various oxidation and reduction reactions.
Recently, a new synthetic route for 5-methylbenzo[b]thiophene has been developed using a one-step amidation reaction of 2-methyl-5-butylthiophene-2-carbaldehyde with an amine, such as piperidine or morpholine, in the presence of a strong acid catalyst, such as sulfuric acid or phosphoric acid.
This reaction results in the formation of 5-methylbenzo[b]thiophene-N-amide, which can then be further reduced to produce 5-methylbenzo[b]thiophene.
One of the advantages of using the above synthetic routes is that they are relatively simple, economical, and environmentally friendly, compared to traditional methods that require expensive and toxic reagents.
Additionally, these routes offer a high yield of the desired product, which is essential for industrial applications.
5-Methylbenzo[b]thiophene has a wide range of applications in the chemical industry, including its use as a pharmaceutical agent, antioxidant, and material for organic electronics.
It has been shown to have anti-inflammatory, anticancer, and antiviral properties, and it has been studied for its potential use in the treatment of various diseases, such as Alzheimer's disease and Parkinson's disease.
In addition to its pharmaceutical applications, 5-methylbenzo[b]thiophene has been widely studied for its potential use as an antioxidant in various industrial applications.
It has been shown to have strong antioxidant properties and has been studied for its potential use in the protection of various materials, such as plastics and textiles, from oxidative degradation.
5-Methylbenzo[b]thiophene is also of interest in the field of organic electronics due to its unique electronic properties.
It has been studied for its potential use in the production of organic field-effect transistors and organic solar cells, and it has been shown to have excellent electronic properties, such as high mobility and high carrier lifetime.
In conclusion, 5-methylbenzo[b]thiophene is an important thiophene derivative with a wide range of applications in the chemical industry.
Its synthetic routes are well established and are commonly used in industrial applications.
Its diverse