Name | 2-Nitrobenzenesulfonyl fluoride |
Molecular Formula | C6H4FNO4S |
Molar Mass | 205.16 g/mol |
Appearance | Solid (usually white or off - white) |
Melting Point | 63 - 65 °C |
Boiling Point | Decomposes before boiling |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
Density | Approx. 1.605 g/cm³ |
Purity Typical | High - purity grades available, e.g., 97%+ |
Flash Point | Non - flammable |
Hazard Class | Corrosive |
What are the main uses of 2-Nitrobenzenesulfonyl fluoride?
2-Nitrobenzenesulfonyl fluoride has a wide range of uses in the chemical industry. First, in the field of organic synthesis, it is an important material for the preparation of sulfonyl compounds. If it meets with alcohols, it can form sulfonates under suitable conditions. This sulfonate is an active intermediate in the organic synthesis path, and can participate in many reactions such as nucleophilic substitution, assisting chemists in constructing complex and delicate organic molecules.
Furthermore, in the field of pharmaceutical chemistry, 2-nitrobenzenesulfonyl fluoride is also important. It can be used to introduce sulfonyl fluoride groups into the molecular structure of drugs. This sulfonyl fluoride group has unique chemical properties, or can improve the physical and chemical properties of drugs, such as solubility, stability, or affinity with biological targets, and help drugs better exert their pharmacological effects.
In the context of materials science, it can be used to synthesize materials with special properties. For example, copolymerization with specific monomers can give materials new characteristics, such as enhancing their chemical stability, surface activity, etc., making materials emerge in many fields such as coatings and film materials to meet the needs of different scenarios.
In summary, 2-nitrobenzenesulfonyl fluoride plays a key role in organic synthesis, medicinal chemistry, materials science and other fields due to its unique chemical properties, promoting the development and progress of various fields, and is indispensable in the chemical industry.
What are the physical properties of 2-Nitrobenzenesulfonyl fluoride?
2-Nitrobenzenesulfonyl fluoride is a unique compound in organic chemistry. Its physical properties are unique, let me explain in detail.
Looking at its properties, under normal circumstances, 2-nitrobenzenesulfonyl fluoride is mostly colorless to light yellow liquid, which makes it different from many solid chemicals in appearance. It shows a flowing state and can flow freely in a specific reaction vessel.
When it comes to odor, it has a relatively special pungent odor. This odor is quite significant. Once it evaporates in the air, it is easily detected by people with a keen sense of smell. This pungent odor not only reflects the chemical activity of the compound, but also prompts that special attention should be paid during use and storage to prevent damage to the human respiratory system.
Let's talk about its melting point. In terms of melting point, it is in a relatively low range, which makes it easy to change from solid to liquid at a slightly higher than the conventional ambient temperature. The boiling point is relatively high, and it needs to reach a certain temperature threshold before it can change from liquid to gaseous. The characteristics of this melting boiling point have a profound impact on its application and operation in various chemical reactions.
Its solubility is also unique. In organic solvents, such as common ether and dichloromethane, 2-nitrobenzenesulfonyl fluoride exhibits good solubility and can be uniformly dispersed, thus creating favorable conditions for related organic synthesis reactions. However, in water, its solubility is poor, due to the characteristics of its molecular structure, which makes it difficult to form an effective interaction with water molecules.
In addition, 2-nitrobenzenesulfonyl fluoride has a density greater than that of water. If it is placed in the same container as water, it will sink to the bottom. This density characteristic is also an important consideration in separation and related experimental operations.
2-Nitrobenzenesulfonyl is fluoride chemically stable?
2-Nitrobenzenesulfonyl fluoride is unstable in nature. Its molecules contain nitro and sulfonyl fluoryl groups, both of which are active. Nitro has strong oxidation, and under certain conditions, it may cause the reaction to go out of control, and the hot topic will even explode. In the sulfonyl fluoride group, the activity of sulfur-fluoride bonds is quite high, and it is easy to initiate nucleophilic substitution reactions when encountering nucleophiles, such as alcohols, amines, and water.
When encountering water, the sulfonyl fluoride group hydrolyzes, forming sulfonic acid first, and then sulfuric acid and hydrofluoric acid. Hydrofluoric acid is highly corrosive and can erode a variety of materials, endangering the safety of the experimenter. In alkaline environments, the reaction rate is faster, and the hydrolysis process is accelerated due to the strong
Under heat or light, the intra-molecular energy of 2-nitrobenzenesulfonyl fluoride increases, the bond energy weakens, or triggers a decomposition reaction. The decomposition products are complex, or contain harmful gases such as nitrogen oxides and sulfur oxides, which not only pollute the environment, but also pose a risk of explosion.
When storing, it is necessary to avoid water, heat and strong light. It should be stored in a cool, dry and well-ventilated place, away from fire, heat sources, oxidants and alkalis. When operating, the experimenter needs to prepare protective equipment and strictly follow the procedures to prevent accidents. In short, 2-nitrobenzenesulfonyl fluoride is chemically active and has poor stability. Caution is required for use and storage.
What are the synthetic methods of 2-Nitrobenzenesulfonyl fluoride?
The synthesis method of 2-nitrobenzene sulfonyl fluoride is quite complicated and requires fine operation. In the past, the following steps were followed.
First, benzene was used as the starting material, and the nitro group was introduced through the nitration reaction. At that time, the mixed acid of concentrated nitric acid and concentrated sulfuric acid was often used as the nitrifying agent, and the ratio, reaction temperature and time of the two needed to be carefully controlled. Benzene and mixed acid were mixed in a specific container and stirred at a suitable temperature. During this process, if the temperature was too high, it was easy to cause frequent side reactions and generate polynitrobenzene impurities. If the temperature was too low, the reaction was slow and the yield was poor. After nitrification, nitrobenzene was obtained.
Second, nitrobenzene was converted into nitrobenzene sulfonic acid. Using fuming sulfuric acid as the sulfonation reagent, this reaction is violent, and the reaction process needs to be carefully added and closely monitored. Nitrobenzene reacts with fuming sulfuric acid under specific conditions to form nitrobenzene sulfuric acid. The concentration and temperature of the reaction system have a great influence on the purity and yield of the product.
Third, to obtain 2-nitrobenzene sulfonyl fluoride, nitrobenzene sulfuric acid needs to be further converted. Phosphorus pentachloride, phosphorus trichloride and other chlorination reagents are often used to convert nitrobenzene sulfuric acid into nitrobenzene sulfonyl chloride. This chlorination reaction needs to be carried out in an anhydrous environment, otherwise it is easy to cause side reactions such as hydrolysis. Subsequently, fluorinated reagents, such as potassium fluoride, are reacted with nitrobenzenesulfonyl chloride to achieve the substitution of chlorine atoms by fluorine atoms, and finally obtain 2-nitrobenzenesulfonyl fluoride. The solvent selection, reaction temperature and other conditions of this substitution reaction also need to be carefully optimized to improve the quality and yield of the product.
Synthesis of 2-nitrobenzenesulfonyl fluoride requires strict control of conditions and attention to detail in each step to obtain satisfactory results.
What are the precautions for 2-Nitrobenzenesulfonyl fluoride in storage and transportation?
2-Nitrobenzenesulfonyl fluoride This material requires attention during storage and transportation.
Its nature is quite active, corrosive and toxic, so when storing, it should be placed in a cool, dry and well-ventilated place. The temperature should be controlled in a lower range to prevent its decomposition or increased reactivity due to excessive temperature, which may cause danger. Be sure to keep away from fires and heat sources, and must not mix with flammable, flammable and reducing substances, as such substances are prone to severe reactions and accidents.
Storage containers must be made of corrosion-resistant materials, such as glass or specific plastic materials, and must be tightly sealed to prevent leakage. After taking it out, the container should be sealed immediately to prevent it from deteriorating due to excessive contact with the air.
During transportation, relevant laws and standards should also be strictly adhered to. The packaging must be strong enough to withstand the vibration and collision of conventional transportation. The transportation vehicle must be equipped with corresponding emergency treatment equipment and protective equipment for emergencies. Transport personnel should be professionally trained and familiar with the characteristics and emergency disposal methods of this substance. Transportation route planning should avoid crowded areas and environmentally sensitive areas, so as to ensure the safety of 2-nitrobenzenesulfonyl fluoride during storage and transportation, and avoid accidental disasters.