Chemical Name: 2-Bromoethanol Molecular Formula: C₂H₅BrO Molecular Weight: 124.97 g/mol CAS Number: 540-51-2
Physical Properties:
Property
Description
Appearance
Colorless to pale yellow liquid
Density
1.658 g/cm³
Boiling Point
146-148°C
Melting Point
-80°C
Solubility
Miscible with water and organic solvents like ethanol and ether
The molecule consists of an ethyl chain with a hydroxyl group (-OH) attached to one carbon and a bromine atom attached to the other. The presence of both functional groups makes it highly reactive, especially in substitution and nucleophilic reactions.
Synthesis
2-Bromoethanol can be synthesized through various methods, one of the most common being the reaction of ethylene oxide with hydrogen bromide (HBr):
This reaction involves the ring opening of ethylene oxide by hydrogen bromide to produce 2-bromoethanol.
Key Applications
Intermediate in Organic Synthesis: 2-Bromoethanol serves as an important intermediate in the synthesis of a wide variety of organic compounds, including pharmaceuticals, agrochemicals, and surfactants. It is used as a starting material for the production of other chemicals due to its reactivity.
Alkylation Agent: The bromine atom in 2-bromoethanol makes it a good leaving group, which allows it to act as an alkylating agent in organic synthesis. It can react with nucleophiles to form various products where the hydroxyl group remains intact or can be further modified.
For instance, 2-bromoethanol can undergo nucleophilic substitution with amines, thiols, or alcohols, forming corresponding ethers, amines, and other derivatives. This is valuable for creating new carbon-carbon or carbon-heteroatom bonds in synthetic pathways.
Epoxide Formation: 2-Bromoethanol can be converted into ethylene oxide, an important intermediate, through dehydrohalogenation. Ethylene oxide is a valuable compound in the production of various industrial chemicals, including ethylene glycol, surfactants, and polyethylene glycols.
Pharmaceutical Synthesis: 2-Bromoethanol is often used in the pharmaceutical industry as a building block in the synthesis of more complex molecules. Its reactivity allows it to be incorporated into drug development pathways, especially in the construction of biologically active compounds like antibiotics and antivirals.
Grignard Reagent Precursor: 2-Bromoethanol can be used to prepare Grignard reagents, which are crucial in organic synthesis. The formation of the Grignard reagent from 2-bromoethanol allows for the introduction of functional groups in subsequent reactions, making it a versatile tool in the construction of complex organic molecules.
Safety and Handling
2-Bromoethanol is hazardous and requires careful handling due to its toxicity and reactivity. The compound is toxic by inhalation, ingestion, and skin contact. It can cause severe irritation to the skin, eyes, and respiratory system. Long-term exposure can have adverse effects on the central nervous system.
Safety Precautions:
Use appropriate personal protective equipment (PPE), such as gloves, safety goggles, and protective clothing.
Work in a well-ventilated area or fume hood to minimize inhalation risks.
Avoid direct contact with the skin and eyes.
In case of exposure, wash the affected area thoroughly with water and seek medical attention if necessary.
Environmental Impact
2-Bromoethanol is harmful to aquatic life and can have long-lasting environmental impacts if not properly handled and disposed of. It should not be released into the environment, and any waste should be treated in accordance with local environmental regulations.
Conclusion
2-Bromoethanol is a useful and versatile chemical intermediate in organic synthesis, widely employed in pharmaceuticals, agrochemicals, and other fine chemicals. Its dual reactivity, due to the bromine and hydroxyl groups, allows it to participate in various organic transformations, making it valuable for alkylation, nucleophilic substitution, and the formation of other functionalized organic molecules. However, due to its toxicity, proper safety measures should be observed during handling and storage.
