Chemical Formula | C2H7N·BF3 |
Molar Mass | 109.89 g/mol |
Appearance | Colorless to pale yellow liquid |
Odor | Pungent |
Density | 1.12 g/cm³ |
Boiling Point | 126 - 129 °C |
Melting Point | -12 °C |
Solubility In Water | Reacts with water |
Solubility In Organic Solvents | Soluble in many organic solvents |
Flash Point | 30 °C |
Stability | Stable under normal conditions, but reacts with water, acids, and bases |
Hazard Class | Corrosive |
What are the main uses of ethylamine-boron trifluoride?
Ethylamine-boron trifluoride is a crucial reagent in organic synthesis. It has a wide range of uses and plays a key role in many chemical fields.
First, in organic synthesis reactions, it is often used as a catalyst. For example, in some esterification reactions, ethylamine-boron trifluoride can accelerate the reaction process and make the reaction more efficient. It can reduce the activation energy of the reaction, which is like building a smoother channel for the chemical reaction and promoting the easier conversion of the reactants into products.
Second, it also has important applications in boronation reactions. The borohydride reaction is an important means to build carbon-boron bonds in organic synthesis, and ethylamine-boron trifluoride can help this reaction proceed smoothly. It can affect the electron cloud distribution of the reaction substrate, thereby regulating the selectivity and rate of the reaction.
Furthermore, ethylamine-boron trifluoride is an indispensable raw material in the preparation of boron-containing organic compounds. With the specific reaction path, it can be used to synthesize various boron-containing organic compounds with novel structures and unique properties, which may have potential application value in materials science, medicinal chemistry and other fields.
Furthermore, in the synthesis strategy of some complex organic molecules, ethylamine-boron trifluoride can ingeniously participate in it and assist in the construction of specific molecular structures. Due to its unique chemical properties, it can precisely interact with other reactants to achieve precise regulation of the structure and properties of the target product.
In short, ethylamine-boron trifluoride occupies a pivotal position in the stage of organic synthetic chemistry due to its diverse functions, providing a powerful tool for chemists to create novel organic compounds and explore unknown chemical fields.
What are the physicochemical properties of ethylamine-boron trifluoride
Ethylamine-boron trifluoride is a commonly used reagent in organic synthesis, with unique physical and chemical properties. Its appearance is usually colorless to light yellow liquid, stable at room temperature and pressure.
The melting point of this compound is quite low, about -126 ° C, which makes it liquid in low temperature environment. This property is very critical in specific low temperature reactions, which is convenient for the control and progress of the reaction. The boiling point is about 125 ° C, and the moderate boiling point makes the separation and purification relatively convenient. It can be effectively separated by controlling the temperature during operations such as distillation.
Ethylamine-boron trifluoride is highly soluble in a variety of organic solvents, such as ether, tetrahydrofuran, etc. Its good solubility is conducive to its dispersion and participation in reactions in different reaction systems, allowing the reactants to fully contact and accelerate the reaction rate.
It has certain chemical activity. Boron trifluoride, as a strong Lewis acid, can react with many compounds containing solitary electrons, such as ethers, alcohols, etc., to form coordination compounds. In the field of organic synthesis, this property is often used to catalyze many reactions, such as the Fu-Ke reaction, which can effectively reduce the activation energy of the reaction and improve the yield and selectivity of the reaction.
However, it should be noted that ethylamine-boron trifluoride is prone to hydrolysis in contact with water, generating corresponding boric acid and ethylamine salts. This hydrolysis reaction may affect its stability and activity in the reaction system. Therefore, it is necessary to avoid water when storing and using it. It is usually operated in a dry inert gas environment to ensure its performance and reaction effect.
What is the preparation method of ethylamine-boron trifluoride?
The method of preparing ethylamine-boron trifluoride follows the following steps.
First take an appropriate amount of boron trifluoride gas, which can be heated by borax and concentrated sulfuric acid, so that borax ($Na_2B_4O_7 $) reacts with concentrated sulfuric acid ($H_2SO_4 $), the chemical equation is $Na_2B_4O_7 + H_2SO_4 + 5H_2O = 4H_3BO_3 + Na_2SO_4 $, boric acid ($H_3BO_3 $) is heated and dehydrated to form boron trifluoride ($B_2O_3 $), $2H_3BO_3\ stackrel {\ Delta }{=\!=\! =} B_2O_3 + 3H_2O $, and then diboron trioxide with fluorite ($CaF_2 $), concentrated sulfuric acid co-heating, $B_2O_3 + 3CaF_2 + 3H_2SO_4\ stackrel {\ Delta }{=\!=\!=} 2BF_3\ uparrow + 3CaSO_4 + 3H_2O $, collect the resulting boron trifluoride gas. < Br >
Another ethylamine, often prepared by co-heating ethanolamine with sodium bromide and concentrated sulfuric acid, ethanolamine ($HOCH_2CH_2NH_2 $) reacts with sodium bromide ($NaBr $) and concentrated sulfuric acid, Mr. Bromoethane ($C_2H_5Br $), $NaBr + H_2SO_4 = HBr + NaHSO_4 $, $HOCH_2CH_2NH_2 + HBr\ stackrel {\ Delta }{=\!=\!=} C_2H_5Br + NH_3\ cdot H_2O $, ethylamine ($C_2H_5NH_2 $) can be obtained by the reaction of bromoethane with ammonia, $C_2H_5Br + NH_3\ stackrel {\ Delta }{=\!=\!=} C_2H_5NH_2 + HBr $.
Then, in a suitable reaction vessel, at a low temperature and in the presence of a suitable catalyst (such as some metal salts supported by activated carbon), slowly introduce boron trifluoride gas into ethylamine, and the two undergo an addition reaction, $C_2H_5NH_2 + BF_3 = C_2H_5NH_2\ cdot BF_3 $, to obtain ethylamine-boron trifluoride. During the reaction, close attention should be paid to the change of temperature to prevent the reaction from being too violent, and the reaction system should be fully stirred so that the two can be uniformly mixed to improve the yield of the product.
What are the precautions for ethylamine-boron trifluoride in storage and transportation?
When storing and transporting ethylamine-boron trifluoride, many things need to be paid attention to.
The first word of storage, because of its lively nature, should be stored in a cool, dry and well-ventilated place. Be sure to keep away from fire and heat sources to prevent danger caused by rising temperature. Because of its sensitivity to air and moisture, it should be ensured that the storage container is tightly sealed to prevent moisture and oxidation. The storage area should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment.
As for transportation, the carrier must have the corresponding qualifications. Before transportation, the packaging must be in good condition and the loading must be safe. During transportation, make sure that the container does not leak, collapse, fall or damage. It is strictly forbidden to mix and transport with oxidizers, acids, etc., as it may react violently with them. When transporting, follow the specified route and do not stop in residential areas and densely populated areas. Transportation vehicles should be equipped with leakage emergency treatment equipment. In the event of leakage, they can be properly disposed of in a timely manner to avoid the expansion of accidents. In short, all aspects of the storage and transportation of ethylamine-boron trifluoride must be carefully operated, and relevant norms and requirements must be strictly followed to ensure safety.
What are the safety risks of ethylamine-boron trifluoride use?
Ethylamine-boron trifluoride is a chemical commonly used in the chemical industry. During its use, many safety risks need to be dealt with with caution.
First, this material is corrosive. Boron trifluoride will react violently in contact with water to form highly corrosive hydrofluoric acid. If it is accidentally exposed to the human body, whether it is the skin or the eyes, it will suffer serious corrosion damage. If the skin touches, it will be as if the body is burned by fire, and it will be red, swollen, painful, and even ulcerated in severe cases. Eye contact may cause vision impairment and even blindness.
Second, there is a risk of toxicity. If the gas volatilized by ethylamine-boron trifluoride is inhaled by the human body, it will cause strong irritation to the respiratory tract. Light can cause coughing and asthma, and severe can cause breathing difficulties and even pulmonary edema, which is life-threatening. Long-term exposure to low concentrations of such gases can also cause chronic damage to the nervous system, liver and other organs.
Third, there is a risk of explosion. Ethylamine is a flammable substance, and it is easy to burn and explode in case of open flames and hot topics. If during use, its vapor and air form an explosive mixture. Once it encounters a fire source, it will be like a volcanic eruption, instantly triggering a violent explosion, causing devastating damage to surrounding facilities and personnel.
Fourth, the risk of uncontrolled reaction cannot be ignored. If the reaction conditions involved in the chemical reaction of ethylamine-boron trifluoride are not properly controlled, such as sudden changes in temperature and pressure, it is very likely to cause the reaction to go out of control, resulting in severe exotherm and gas generation, which in turn causes the reaction vessel to break and cause more serious accidents.
Therefore, when using ethylamine-boron trifluoride, it is necessary to strictly follow the safety operating procedures and take protective measures to ensure the safety of personnel and the environment.