-
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-chlorothiophene-3-carboxylic acid, also known as 3-chlorothiophene-2-carboxylic acid, is a key step in the manufacture of various chemicals and pharmaceuticals.
This acid is a colorless liquid with a pungent odor, and it is commonly used as an intermediate in the production of various compounds, such as herbicides, insecticides, and pharmaceuticals.
The production process of 2-chlorothiophene-3-carboxylic acid involves several steps, including synthesis, purification, and isolation.
In this article, we will discuss the production process of 2-chlorothiophene-3-carboxylic acid in detail, highlighting the key steps and challenges involved in the manufacturing process.
Synthesis of 2-chlorothiophene-3-carboxylic acid
The synthesis of 2-chlorothiophene-3-carboxylic acid involves several steps, including the reaction of thiophene-2-carboxylic acid with chloroform, followed by a series of other reactions to convert the resulting intermediate into the final product.
The synthesis process can be illustrated as follows:
Thiophene-2-carboxylic acid + Chloroform → 2-chlorothiophene-3-carboxylic acid
The reaction between thiophene-2-carboxylic acid and chloroform is carried out in the presence of a solvent, such as dichloromethane, and a catalyst, such as hydrochloric acid.
After the reaction is complete, the mixture is filtered to remove any solid impurities, and the resulting liquid is washed with water to remove any trace amounts of the catalyst.
The purified liquid is then treated with sodium hydroxide, which converts the carboxylic acid into a sodium salt.
The salt is then extracted with a solvent, such as ether, and the resulting organic layer is separated and dried.
The residue is then heated with a solvent, such as benzene, to remove any remaining impurities.
Purification of 2-chlorothiophene-3-carboxylic acid
After the synthesis step, the 2-chlorothiophene-3-carboxylic acid product is typically impure and contains other organic compounds that need to be removed.
The purification process involves several steps, including crystallization, distillation, and chromatography.
Crystallization involves cooling the impure product to a low temperature, causing the impurities to precipitate out of solution, leaving behind a pure form of 2-chlorothiophene-3-carboxylic acid.
Distillation involves heating the impure product to separate the components based on their boiling points.
The resulting fractions are then collected and analyzed to determine their purity.
Chromatography is a technique that involves passing the impure product through a column packed with a solid material, such as silica gel or alumina.
The components of the mixture interact differently with the solid material, causing them to separate as they pass through the column.
The resulting fractions are then collected and analyzed to determine their purity.
Isolation of 2-chlorothiophene-3-carboxylic acid
After the purification process, the 2-chlorothiophene-3-carboxylic acid product is typically isolated as a solid or a liquid.
The isolation process may involve several steps, including recrystallization, filtration, and drying.
Recrystallization involves dissolving the purified 2-chlorothiophene-3-carboxylic acid in a suitable solvent, such as dichloromethane or ethyl