Catalog Number | ACM93102057-1 |
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CAS Number | 93102-05-7 |
Structure | ![]() |
Molecular Weight | 237.41 g/mol |
Molecular Formula | C13H23NOSi |
Boiling Point | 76 °C(0.3 mmHg) |
Flash Point | 66 °C |
Purity | ~90% |
Density | 0.928-0.936 g/mL |
Appearance | Colorless to light yellow clear liquid |
Application | N-(Methoxymethyl)-N-(Trimethylsilylmethyl)Benzylamine serves as a critical reagent in the synthesis of N-benzyl substituted pyrrolidines through [3+2] cycloaddition reactions with αβ-unsaturated esters This reagent is highly valued for its ability to generate N-benzyl azomethine ylide in situ utilizing catalysts such as trifluoroacetic acid for efficient reactivity N-(Methoxymethyl)-N-(Trimethylsilylmethyl)Benzylamine is preferred for its ease of handling compared to alternative silylmethylamine precursors The reactive intermediate produced in this process acts as a 13-dipolar species facilitating reactions with electron-deficient alkenes and alkynes to form pyrrolidine derivatives 3-pyrrolines and pyrroles The specificity of cycloaddition ensuring complete cis stereospecificity contributes to convergent pathways in forming diverse pyrrolidine structures This reagent is particularly significant in large-scale practical syntheses of chiral pyrrolidines and 3-carboxy-1-azabicyclo[221]heptane derivatives which are notable for their physiological activity |
Storage | Keep in dark place,Sealed in dry,Room Temperature |
Hazardous Materials Information | Not hazardous material |
MDL Number | MFCD00674005 |
Packaging | 1 g |
Efficient and Versatile Reagent for Pyrrolidine Synthesis
After using N-(Methoxymethyl)-N-(Trimethylsilylmethyl)Benzylamine from Alfa Chemistry, I found it easy to handle and effective in synthesizing pyrrolidines via [3+2] cycloaddition for my research. Highly recommended for precision in chemical synthesis.
※ Please kindly noted that this product is for research use only.