-
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
7-Bromo-1-heptanol is an important organic compound that finds wide application in the chemical industry.
It is used as an intermediate in the synthesis of various chemicals, drugs, and other products.
The synthetic routes for 7-bromo-1-heptanol can be broadly classified into two categories, namely, synthetic routes that involve the use of halogen compounds and those that do not.
Synthetic Routes Involving Halogen Compounds:
The most common method of synthesizing 7-bromo-1-heptanol involves the use of halogen compounds such as bromine or chlorine.
The reaction is generally carried out in the presence of a solvent such as ether or dichloromethane.
The reaction involves the addition of bromine or chlorine to 1-heptanol, which is first treated with an acid catalyst such as hydrochloric acid or sulfuric acid.
This reaction is highly exothermic and must be carried out with caution.
The reaction mixture is then treated with a Base such as sodium hydroxide or potassium hydroxide to neutralize the acid catalyst.
The product is then extracted with a solvent such as ether or dichloromethane and the organic phase is separated, dried and concentrated to yield 7-bromo-1-heptanol.
Synthetic Routes Not Involving Halogen Compounds:
An alternative method of synthesizing 7-bromo-1-heptanol involves the use of reagents such as lithium aluminum hydride (LiAlH4) or sodium hydride (NaH).
The reaction is carried out in the presence of a solvent such as ether or THF.
In this reaction, 1-heptanol is first treated with LiAlH4 or NaH, which deprotonates the alpha-carbon to form an enolate.
This enolate is then treated with bromine or chlorine to form the bromide or chloride of 7-bromo-1-heptanol.
The product is then extracted with a solvent such as ether or THF and the organic phase is separated, dried and concentrated to yield 7-bromo-1-heptanol.
Advantages of synthetic routes not involving halogen compounds:
The synthetic routes not involving halogen compounds have several advantages over the traditional methods that use halogen compounds.
One of the main advantages is that they are less hazardous to handle and dispose of, as halogen compounds are known to be highly toxic and corrosive.
Additionally, the reactions are generally milder and more efficient, which leads to higher yields of the desired product.
Applications of 7-Bromo-1-heptanol:
7-Bromo-1-heptanol is used as an intermediate in the synthesis of various chemicals, drugs, and other products.
It is used in the production of fragrances, flavors, and other consumer products.
It is also used as a building block for the synthesis of antibiotics, anti-inflammatory drugs, and other pharmaceuticals.
Its ability to undergo further reactivity makes it a versatile building block in organic synthesis.
In conclusion, 7-bromo-1-heptanol is an important organic compound that finds wide application in the chemical industry.
It can be synthesized through a variety of methods, some of which involve the use of halogen compounds and others that do not.
The synthetic routes that do not involve halogen compounds are generally considered to be safer and more efficient.
Additionally, 7-bromo-1-heptanol is used as an intermediate in the synthesis of various chemicals, drugs, and other products.