2 Dimethylamino Pyridine 5 Boronic Acid Pinacol Ester
pyridine pyrrole pyrazine piperidine piperazine

2-(Dimethylamino)pyridine-5-boronic acid pinacol ester

    Specifications

    HS Code

    742508

    Chemical Formula C13H21BN2O2
    Molecular Weight 248.13
    Appearance Solid (Typical)
    Purity Typically high - 95%+ (Common in lab - grade)
    Solubility In Organic Solvents Soluble in many organic solvents like dichloromethane, toluene
    Melting Point 110 - 114 °C (Approximate)
    Storage Condition Store in a cool, dry place, protected from moisture
    Reactivity Reactive towards electrophiles, can participate in cross - coupling reactions
    Odor Odorless or very faint odor
    Sensitivity Sensitive to air and moisture to some extent

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    General Information
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    Frequently Asked Questions

    As a leading 2-(Dimethylamino)pyridine-5-boronic acid pinacol ester supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the main use of 2- (Dimethylamino) pyridine-5-boronic acid pinacol ester
    2-%28Dimethylamino%29pyridine-5-boronic acid pinacol ester is an important intermediate in organic synthesis. It has a wide range of uses and is often a key building block for the construction of drug molecules in the field of medicinal chemistry. Due to its unique reactivity of boron ester structure, it can be combined with many electrophilic reagents through various coupling reactions, so that various functional groups can be easily introduced to help build complex drug frameworks.
    In the field of materials science, this compound also has its uses. It can be used as a raw material for the synthesis of functional materials. Through precise chemical modification, the material is endowed with specific photoelectric properties or other special properties to meet the needs of different application scenarios.
    In the field of organic synthetic chemistry, it is often used to form carbon-carbon bonds or carbon-heteroatom bonds. Through classical organic reactions such as Suzuki-Miyaura coupling reaction, it reacts with substrates such as halogenated aromatics or halogenated heteroaromatics to realize arylation or heteroarylation processes, providing an effective path for the synthesis of organic compounds with diverse structures, thereby promoting the development of new organic materials and drugs.
    2- (Dimethylamino) pyridine-5-boronic acid pinacol ester
    2-%28Dimethylamino%29pyridine-5-boronic+acid+pinacol+ester that is, 2 - (dimethylamino) pyridine - 5 - boronic acid pinacol ester, the synthesis method is as follows:
    First, 2 - chloro - 5 - bromopyridine is used as the starting material. In a suitable reaction vessel, the corresponding solution of dimethylamine is added. Under the action of a certain temperature and base, a nucleophilic substitution reaction occurs. The chlorine atom is replaced by dimethylamino to obtain 2- (dimethylamino) - 5 - bromopyridine. In this step, the temperature needs to be precisely controlled, and the type and dosage of base also have a great impact on the reaction process and yield. Subsequently, 2 - (dimethylamino) -5 - bromopyridine and diphenacol borate are mixed into the reaction system, and suitable palladium catalysts and ligands are added. In the presence of a base, an inert gas is introduced to protect, and boronation is carried out at temperature, and finally 2 - (dimethylamino) pyridine - 5 - boronic acid phenacol ester is formed. In this process, factors such as palladium catalyst activity, ligand structure and the anaerobic environment of the reaction system all play a key role in the success of the reaction.
    Another approach is to start from 2 - (dimethylamino) pyridine, introduce a specific positioning guide group, activate the hydrogen atom at the 5th position on the pyridine ring, and then react with boron-containing reagents under mild conditions to achieve boronation at the 5th position, and then react with pinacol to form the target product 2 - (dimethylamino) pyridine - 5 - boronic acid pinacol ester. The key to this method lies in the selection of positioning guide groups and subsequent removal, as well as the optimization of boronation reaction conditions.
    What are the physical and chemical properties of 2- (Dimethylamino) pyridine-5-boronic acid pinacol ester
    2-%28Dimethylamino%29pyridine-5-boronic acid pinacol ester has many physical and chemical properties. Its appearance is often white to off-white solid powder, which is conducive to discrimination. The value of the melting point, about a specific range, is one of its important characteristics. The method of measuring the melting point can be used to identify this substance.
    In terms of solubility, it can show a certain solubility in organic solvents, such as common tetrahydrofuran and dichloromethane. This property is relevant to its good participation in the reaction process in organic synthesis, which has a great impact.
    Stability cannot be ignored. Under normal environmental conditions, this compound has certain stability. However, when it encounters strong oxidizing agents, strong acids or strong bases, the stability is easily damaged, and chemical reactions occur, resulting in structural and property changes.
    Its molecular structure contains specific functional groups, pyridine ring, dimethylamino group and boric acid pinacol ester group. Each functional group has unique chemical activities, enabling the compound to participate in a variety of chemical reactions, such as coupling reactions, etc., and has a wide range of uses in the field of organic synthesis.
    In addition, its spectral properties also have characteristics. Infrared spectroscopy, nuclear magnetic resonance spectroscopy, etc., can provide key information for determining its structure and purity. The specific absorption peaks in infrared spectroscopy can characterize the vibrational characteristics of functional groups; the chemical shifts and coupling constants of each peak in nuclear magnetic resonance spectroscopy can reveal the connection patterns and environments of hydrogen atoms and other atoms in molecules.
    2- (Dimethylamino) pyridine-5-boronic acid pinacol ester during storage and transportation
    2-%28Dimethylamino%29pyridine-5-boronic acid pinacol ester, it is also a chemical substance. When storing and transporting, there are several things to pay attention to.
    First words storage, this compound should be stored in a cool, dry and well ventilated place. It covers its properties or changes due to temperature and humidity. High temperature or cause it to decompose, and humid gas can also cause it to deteriorate, so hot topic and moisture must be avoided.
    Furthermore, keep away from fire sources, heat sources and oxidants. This compound encounters open flames, hot topics or mixing with oxidants, or the risk of combustion or explosion. Therefore, in the storage place, fireworks are strictly prohibited, and they are placed separately from oxidants to prevent accidents.
    When transporting, also be cautious. Make sure that the packaging is intact to prevent leakage. If it is contained in a container, the material of the container must be resistant to the erosion of this compound, and it must be tightly sealed. During transportation, severe vibration and collision should be avoided to avoid damage to the packaging.
    In addition, the transport vehicle should also be selected appropriately, the ventilation in the car must be good, and there are fire and explosion-proof equipment. The escort should be aware of the characteristics of this compound and emergency disposal methods, so as not to be in danger.
    In general, 2-%28Dimethylamino%29pyridine-5-boronic acid pinacol ester must be stored and transported according to its chemical properties and strictly abide by relevant regulations to ensure safety.
    2- (Dimethylamino) pyridine-5-boronic acid pinacol ester market price and market prospects
    Today there are 2 - (dimethylamino) pyridine - 5 - boronic acid pinacol ester, its market price and market prospects. This compound is very important in the field of organic synthesis, often used as a catalyst or intermediate.
    When it comes to market prices, they vary according to quality, purity, supply and demand situation and manufacturers. High purity, due to the complicated preparation process, strict requirements for raw materials and equipment, the price is naturally expensive. For small-scale scientific research purposes, its price may be in grams, or up to tens of yuan to more than 100 yuan per gram. If it is for large-scale industrial production needs, when purchasing in batches, the price per kilogram or due to large discounts can be reduced to several thousand yuan.
    As for the market prospect, organic synthetic chemistry is developing rapidly, and the demand for it in the fields of new drug research and development, materials science and other fields continues to grow. In the research and development of new drugs, it helps to build complex pyridine compound structures and promotes the creation of innovative drugs. In materials science, it is used to synthesize materials with special optoelectronic properties. With the expansion of related industries, its market demand is expected to rise. However, the market competition is also fierce, and new synthesis methods and alternative products may pose challenges to its market share. Overall, with its application in key fields, the market prospect of 2 - (dimethylamino) pyridine - 5 - boronic acid pinacol ester may still be broad in the future. It is only necessary to pay attention to technological innovation and market dynamics to cope with changes.