Diethyl 2 2 4 Difluorophenyl Prop 2 En 1 Yl Malonate
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
Diethyl [2-(2,4-difluorophenyl) prop-2-en-1-yl]malonate
Chemical Formula C17H20F2O4
Molecular Weight 326.34
Chemical Formula C17H20F2O4
Molecular Weight 326.335 g/mol
Chemical Name Diethyl [2-(2,4-difluorophenyl)prop-2-en-1-yl]malonate
Molecular Formula C16H18F2O4
Molecular Weight 312.31
Chemical Formula C17H20F2O4
Molecular Weight 326.34
Appearance Solid (usually)
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in some organic solvents like ethanol, chloroform
Vapor Pressure Low
FAQ

What is the chemical structure of Diethyl [2- (2,4-difluorophenyl) prop-2-en-1-yl] malonate?

The structure of this compound can be analyzed from its name. "Diethyl [2- (2,4-difluorophenyl) propylene-2-enyl-1-yl] malonate", in which "diethylmalonate" is the main structure, and the two carboxyl groups of malonate are estered with ethanol, so two ethoxy-OC ² H are attached to the carboxyl carbon of the central malonate. And the "[2- (2,4-difluorophenyl) propylene-2-enyl-1-yl]" part is the substituent. " 2-Alene-1-yl "indicates that the substituent is a propyl group containing a double bond, and the double bond is located in the 2nd carbon position." 2 - (2,4-difluorophenyl) "indicates that the 2nd carbon position of the propyl group is connected with a phenyl group, and the 2nd and 4th positions of the phenyl group are each connected with a fluorine atom.

In summary, the structure of this compound has a malonate structure in the center, and the carboxyl groups on both sides are esterified by ethoxy. One side of methylene is connected to a propyl group containing a double bond, and the 2nd carbon position of the propyl group is connected with a 2,4-difluorophenyl group. This structure is in line with the chemical structure information contained in its complex naming.

What are the main uses of Diethyl [2- (2,4-difluorophenyl) prop-2-en-1-yl] malonate

This compound is called diethyl [2- (2,4-difluorophenyl) propane-2-ene-1-yl] malonate, and its main use is not recorded in Tiangong Kaiji, but according to today's chemical knowledge, in the field of organic synthesis, it can be used as a key intermediate to construct complex organic molecular structures. Because of its specific chemical structure, it contains alkenyl and malonate ester groups, which can introduce different functional groups into molecules through various reactions, such as the substitution reaction with nucleophilic testers, so as to synthesize bioactive compounds. In pharmaceutical research and development, it may help to synthesize new drug molecules. In materials science, through appropriate reaction transformation, polymer materials with special properties may be prepared, because their structures can endow materials with unique physical and chemical properties. In addition, in the synthesis of fine chemicals, such as synthetic fragrances, pesticides, etc., it may also be used as an important raw material to use its structural characteristics through specific reaction routes to produce target fine chemicals and improve product performance and quality.

What are the synthesis methods of Diethyl [2- (2,4-difluorophenyl) prop-2-en-1-yl] malonate

The method of preparing diethyl [2- (2,4-difluorophenyl) propane-2-enyl-1-yl] malonate is often followed by several methods. One method starts with 2,4-difluorobenzaldehyde, which is co-placed with diethyl malonate and a base in an appropriate solvent. The base can initiate the active methylene of diethyl malonate, so that it can condensate with 2,4-difluorobenzaldehyde and produce enylation products. Among them, the nature of the solvent is quite critical to the reaction. Commonly used are ethanol, toluene, etc., which can help the reactants to dissolve and facilitate the reaction. The alkali can be selected from piperidine, pyridine and the like, and the dosage should be precisely controlled. If the amount is small, the reaction will be delayed, and if the amount is large or the side effect should be introduced.

Another method can be used to carry out nucleophilic substitution reaction with the help of metal catalysts and bases. Metal catalysts such as palladium and copper can activate the carbon-halide bond of the halogen, making it easy for nucleophiles to attack. The base can neutralize the generated hydrogen halide and keep the reaction in a positive direction. The temperature and time of the reaction must also be carefully observed. If the temperature is low, the reaction will not be complete, and if it is high, the product may be decomposed.

In addition, the target is also prepared by the addition reaction of 2,4-difluorophenylpropane and diethyl malonate under an appropriate catalytic system. The catalytic system or the transition metal-containing complex can promote the addition of the alkylene bond and diethyl malonate. In this process, the screening of the catalyst and the ratio of the reactants need to be carefully studied to obtain the product with excellent yield and purity.

All these methods have advantages and disadvantages. In practice, according to the availability of raw materials, the ownership of equipment, and the consideration of cost, etc., choose the best one and follow it, so that the reaction is smooth and the product is suitable.

What are the physical properties of Diethyl [2- (2,4-difluorophenyl) prop-2-en-1-yl] malonate

Diethyl [2 - (2,4 - difluorophenyl) propane-2-enyl-1-yl] malonate is one of the organic compounds. Its physical properties are crucial and play an important role in many chemical processes and applications.

The properties of this compound are mostly liquid at room temperature and pressure. Looking at its appearance, it may be a colorless to light yellow transparent liquid with uniform and clear texture and no impurities visible to the naked eye.

Its density is greater than that of water, at room temperature, it is about [X] grams per cubic centimeter. This density characteristic makes it sink when it is in water. The boiling point of

is related to its volatility. The boiling point of this substance is about [X] ° C. This value indicates that it needs a higher temperature to convert into a gaseous state, and the volatility is relatively weak. The melting point of

is also an important physical parameter. Its melting point is about [X] ° C. When the temperature drops below the melting point, the compound will change from a liquid state to a solid state.

In terms of solubility, the substance exhibits good solubility in organic solvents such as ethanol and ether, but its solubility in water is quite limited. This characteristic is due to the characteristics of the organic groups in its molecular structure, which makes it interact weakly with water molecules.

In addition, the refractive index of the compound also has a specific value, which is about [X]. This parameter reflects its ability to refract light, which may have certain reference value in the research and application field of optics. The above physical properties are interrelated and affect each other, and together determine the behavior and application of diethyl [2 - (2,4 - difluorophenyl) propylene - 2 - ene - 1 - yl] malonate in chemical systems.

What are the precautions for Diethyl [2- (2,4-difluorophenyl) prop-2-en-1-yl] malonate in storage and transportation?

Fudiethyl [2- (2,4-difluorophenyl) propane-2-enyl-1-yl] malonate is an important compound in organic chemistry. During storage and transportation, many matters need to be paid attention to.

The first to bear the brunt is the temperature of the storage environment. This compound is quite sensitive to temperature, and high temperature can easily cause its chemical properties to change, or cause adverse reactions such as decomposition. Therefore, it should be stored in a cool place. Generally speaking, the temperature should be maintained between 15 ° C and 25 ° C. In this way, the stability of its chemical structure can be ensured, and it will not deteriorate due to excessive temperature.

Second, humidity is also a key factor. A humid environment can make the compound absorb moisture, which in turn affects its purity and quality. Therefore, the storage must be kept dry, and the relative humidity should be controlled between 40% and 60%. A dry storage atmosphere can be created by auxiliary means such as desiccants.

Furthermore, when transporting, be sure to take protective measures. Because it may have certain chemical activity, vibration and collision may affect it. The packaging must be strong and shockproof to prevent damage to the container due to bumps during transportation, causing leakage and other dangers.

In addition, this compound may be sensitive to light. Exposure to strong light for a long time may cause it to undergo photochemical reactions, resulting in changes in properties. Therefore, during storage and transportation, direct exposure to strong light should be avoided, and light-shielding packaging materials can be used to properly protect it.

In summary, the storage and transportation of diethyl [2- (2,4-difluorophenyl) propylene-2-alkene-1-yl] malonate requires attention to temperature, humidity, protection and shading to ensure its quality and safety.