Name | 3 - Chlorothiophene |
Molecular Formula | C4H3ClS |
Molecular Weight | 118.58 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 149 - 150 °C |
Melting Point | -40 °C |
Density | 1.267 g/cm³ |
Flash Point | 45 °C |
Solubility In Water | Insoluble |
Vapor Pressure | 1.33 kPa (37.7 °C) |
Refractive Index | 1.567 |
What are the physical properties of 3-chlorothiophene?
3-Bromopentane is an organic compound, and its physical properties are quite unique. Looking at its appearance, under room temperature and pressure, it is a colorless to light yellow transparent liquid, clear and with a certain fluidity. Its odor is slightly irritating, but it is not extremely strong and pungent.
When it comes to the boiling point, the boiling point of 3-bromopentane is about 137-139 ° C. This boiling point value means that at this temperature, 3-bromopentane will be converted from liquid to gaseous state. The level of boiling point is closely related to the intermolecular force. There is a van der Waals force between the molecules of 3-bromopentane. Due to the existence of bromine atoms, the intermolecular force is enhanced, so the boiling point is relatively moderate.
In terms of melting point, it is about -95 ° C. When the temperature drops below the melting point, 3-bromopentane condenses from a liquid state to a solid state. The melting point is low, indicating that 3-bromopentane is in a liquid state at room temperature.
Density is also one of the important physical properties, and its density is greater than that of water, about 1.21 g/mL. This causes 3-bromopentane to sink to the bottom of the water when mixed with water, forming a layered situation.
In terms of solubility, 3-bromopentane is insoluble in water. This is because water is a polar molecule, while 3-bromopentane is a non-polar or weakly polar molecule. According to the principle of "similar miscibility", the two are difficult to dissolve each other. However, 3-bromopentane is soluble in many organic solvents, such as ethanol, ether, acetone, etc., and is often used as a reaction medium in organic synthesis reactions.
In addition, the volatility of 3-bromopentane is relatively moderate. Although it is not as volatile as some low-boiling and high-volatility substances, it will also evaporate after a certain period of time in an open environment. This requires that when storing and using 3-bromopentane, care should be taken to seal it to prevent it from volatilizing and escaping.
What are the chemical properties of 3-chlorothiophene?
3-Bromopentane is an organic compound with the commonality of haloalkanes. Its physical properties are colorless to light yellow liquid at room temperature, with a special odor, insoluble in water, and miscible with organic solvents such as ethanol and ether.
In terms of its chemical properties, the nucleophilic substitution reaction is the first. Due to the strong electronegativity of bromine atoms, the polarity of carbon-bromine bonds is quite large, which makes the electron cloud density of carbon atoms connected to bromine reduced and vulnerable to attack by nucleophiles. For example, when co-heated with an aqueous solution of sodium hydroxide, the bromine atom is replaced by a hydroxyl group to form pentanol. The reaction formula is:\ (C_ {5} H_ {11} Br + NaOH\ xrightarrow [] {H_ {2} O} C_ {5} H_ {11} OH + NaBr\).
And the elimination reaction. Under the heating condition of potassium hydroxide alcohol solution, 3-bromopentane will undergo elimination reaction, and the bromine atom and the hydrogen atom on the adjacent carbon atom are removed in the form of hydrogen bromide to form pentene. If there are two different hydrogen atoms in the adjacent carbon atoms, according to Zaitsev's rule, the main product is the olefin with more hydrocarbon groups on the double-bonded carbon atoms, that is, 2-pentene. The reaction formula is:\ (C_ {5} H_ {11} Br + KOH\ xrightarrow [] {alcohol,\ triangle} C_ {5} H_ {10} + KBr + H_ {2} O\).
In addition, 3-bromopentane can also react with metallic magnesium in anhydrous ether to form Grignard reagents. Grignard reagent is extremely reactive and can react with a variety of carbonyl-containing compounds for the construction of carbon-carbon bonds, which is of great significance in the field of organic synthesis. If it reacts with formaldehyde, the corresponding alcohol can be obtained after hydrolysis, which is an important method for growing carbon chains.
What are the main uses of 3-chlorothiophene?
3-Bromopropane is a commonly used raw material in organic synthesis and has important uses in many fields.
First, it plays a significant role in the field of pharmaceutical synthesis. For example, when synthesizing some drugs with specific physiological activities, 3-bromopropane can be used as a key intermediate. Taking the synthesis of a certain type of antiarrhythmic drug as an example, the introduction of specific groups in its molecular structure is often achieved by the reaction involving 3-bromopropane. By substitution reaction with compounds containing specific functional groups, the complex structure of the drug can be gradually constructed, which can give the drug the required pharmacological activity.
Second, it is also indispensable in the preparation of pesticides. The synthesis of many efficient pesticides relies on 3-bromopropane. For example, during the synthesis of some organophosphorus pesticides, 3-bromopropane can react with phosphorus-containing compounds to form pesticide active ingredients with insecticidal and herbicidal effects. It plays an important role in connecting different functional groups, adjusting molecular polarity and activity in the construction of pesticide molecular structures, so as to improve the effect of pesticides on target organisms.
Third, in the field of materials science, 3-bromopropane is also used. For example, when preparing some polymer materials with special properties, the active bromine atom of 3-bromopropane can be used to initiate polymerization reactions or as a reaction check point for cross-linking agents. By copolymerizing with other monomers, the physical properties of polymer materials can be improved, such as improving the flexibility and corrosion resistance of materials, thereby expanding the application range of polymer materials in different fields.
In addition, 3-bromopropane is also a commonly used reagent in the basic research of organic synthetic chemistry. Researchers often use it as a starting material to study various organic reaction mechanisms, explore new reaction paths and methods, and provide a theoretical and practical basis for the development of organic synthetic chemistry.
What are the synthesis methods of 3-chlorothiophene?
There are many methods for synthesizing 3-bromopentane, each with its own advantages and disadvantages. When choosing, it should be weighed according to specific needs and conditions. The common ones are listed as follows:
1. ** Substitution reaction of alcohol and hydrobromic acid **: Pentanol and hydrobromic acid are used as raw materials, sulfuric acid is used as a catalyst, and the substitution reaction occurs to generate 3-bromopentane. This reaction mechanism is that the bromine ion in hydrobromic acid attacks the carbon atom attached to the alcohol hydroxyl group, and the hydroxyl group binds to the proton and leaves in the form of water to complete the substitution. The advantage is that the raw material is common and easy to obtain, and the operation is not complicated; the disadvantage is that the reaction may produce by-products, and the post-reaction treatment may require fine operation to purify the product. < br ** Addition reaction of olefins and hydrogen bromide **: Select a suitable pentene, such as 2-pentene, to undergo an addition reaction with hydrogen bromide. Following the Markov rule, hydrogen atoms are added to double-bonded carbon atoms containing more hydrogen, and bromine atoms are added to double-bonded carbon atoms containing less hydrogen to obtain 3-bromopentane. The advantage of this method is that the reaction steps are simple and the yield is usually high; however, the preparation of olefin feedstocks may require additional steps, and if there are impurities or improper control of reaction conditions, other addition products may be produced.
3. ** Substitution reaction of halogenated hydrocarbons **: A suitable halopentane, such as 3-chloropentane, can be selected, and a halogen exchange reaction occurs with sodium bromide in an appropriate solvent (such as acetone) to generate 3-bromopentane. This reaction is based on the difference in nucleophilic substitution activity of halogen ions, and bromine ions replace chlorine atoms. The advantage is that the reaction conditions are relatively mild; however, the choice of raw materials halopentane may be limited, and the solvent selection and post-treatment also need to be carefully considered.
These several methods for synthesizing 3-bromopentane have their own advantages. In practical application, it is necessary to consider factors such as raw material availability, cost, reaction conditions, product purity, etc., and carefully choose to achieve the best synthesis effect.
What are the precautions for 3-chlorothiophene during storage and transportation?
3 - In the process of storage and storage, it is necessary to pay attention to all kinds of things. The soil is special, the content is high, and the acidity is constant. It is the first to prevent moisture during storage. Because of its absorbency, if it is damp, it will dissolve and shift, and it will not change the composition, which may also affect its original use. Therefore, it should be stored in a sealed container to prevent intrusion.
In addition, the degree of storage in the earth also needs to be controlled. The degree of storage can cause crystallization and precipitation, which can affect its quality. Usually, it is appropriate to maintain the phase stability to avoid high or low end.
It must be solid and reliable. Due to the corrosive nature of multi-layer materials, the packaging materials need to be corrosion-resistant, such as special plastic materials or anti-corrosive gold containers, to prevent the package from breaking and leaking during the process.
The cleaning of the tool should not be ignored. Before use, it is necessary to clean the bottom to remove the residue that may be damaged. If it is not damaged or caused by chemical reactions, it will endanger the safety of the product and also affect the quality of the product.
In addition, the road should be comprehensive. Avoid the areas that are prone to water and tide, and reduce the damage caused by moisture. At the same time, consider the traffic problem, and strive to save the distance, shorten the time, and reduce the shadow of external factors. In this way, it is necessary to properly store the land and ensure the efficiency of the use of its products.