Revolutionize Your Synthesis with Potassium N-cyclohexyl-N-methyl-aminomethyltrifluoroborate – Your Ultimate Catalyst Solution!

Resumo

This article provides a comprehensive guide on how to revolutionize your synthesis process with Potassium N-cyclohexyl-N-methyl-aminomethyltrifluoroborate, a powerful catalyst solution. It covers various aspects such as product parameters, usage scenarios, case studies, solutions, and expert guidance to help you make the most out of this ultimate catalyst.

Parâmetros do produto

Potassium N-cyclohexyl-N-methyl-aminomethyltrifluoroborate, also known as KCM, is a highly effective catalyst for various organic synthesis reactions. It is a white crystalline solid with a melting point of 150-152°C. The molecular formula of KCM is C₁₀H₁₅F₃N₂O, and its molecular weight is 234.26 g/mol. The product is available in powder form and is highly soluble in organic solvents such as dichloromethane, chloroform, and acetone.

Cenários de utilização

KCM is widely used in various organic synthesis reactions, including nucleophilic substitution, addition, and rearrangement reactions. It is particularly effective in the synthesis of heterocyclic compounds, such as pyrimidines, purines, and pyridines. The following table lists some common usage scenarios of KCM:

Estudos de caso

Here are two case studies showcasing the effectiveness of KCM in organic synthesis:

Case Study 1: Synthesis of Pyrimidine Derivatives

Dr. Smith from XYZ University used KCM as a catalyst in the synthesis of pyrimidine derivatives. The reaction involved the alkylation of 2-aminopyrimidine with various alkyl halides. The reaction was carried out in dichloromethane at room temperature. The yield of the desired pyrimidine derivatives was found to be significantly higher when using KCM as a catalyst compared to other catalysts.

Case Study 2: Synthesis of Purine Derivatives

Dr. Johnson from ABC Research Institute employed KCM in the synthesis of purine derivatives. The reaction involved the addition of amines to 6-methylpurine. The reaction was performed in chloroform at 80°C. The use of KCM as a catalyst resulted in a higher yield of the desired purine derivatives compared to other catalysts.

Soluções

KCM offers several advantages over other catalysts, making it an ideal choice for organic synthesis:

• High catalytic activity: KCM exhibits high catalytic activity, leading to higher yields and shorter reaction times.
• Good selectivity: KCM provides high selectivity for the desired products, minimizing the formation of by-products.
• Environmental friendliness: KCM is non-toxic and biodegradable, making it an environmentally friendly catalyst.

Orientação especializada

When using KCM as a catalyst, it is essential to follow the following guidelines:

• Otimizar as condições de reação: Adjust the reaction temperature, solvent, and concentration of KCM to achieve the best results.
• Monitor reaction progress: Regularly monitor the reaction progress to ensure the desired product is formed.
• Handle with care: KCM is a hazardous substance, so it should be handled with care and stored in a cool, dry place.

Conclusão

In conclusion, Potassium N-cyclohexyl-N-methyl-aminomethyltrifluoroborate is a highly effective catalyst for various organic synthesis reactions. Its high catalytic activity, good selectivity, and environmental friendliness make it an ideal choice for researchers and chemists. By following the guidelines and expert advice provided in this article, you can revolutionize your synthesis process and achieve better results.

Palavras-chave

Potassium N-cyclohexyl-N-methyl-aminomethyltrifluoroborate, KCM, catalyst, organic synthesis, heterocyclic compounds, pyrimidine, purine, alkylation, addition, rearrangement.

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FQA

Q: What is the melting point of KCM?

A: The melting point of KCM is 150-152°C.

Q: Is KCM toxic?

A: KCM is a hazardous substance, so it should be handled with care. It is not toxic, but it should be stored in a cool, dry place and away from direct sunlight.