1821-99-4

Usage

Uses

Used in Organic Synthesis:
N,N'-bis(trimethylsilyl)ethylenediamine is used as a reagent for its ability to protect nitrogen atoms in organic synthesis, preventing unwanted side reactions and facilitating the formation of desired products.
Used in Metal-Catalyzed Reactions:
In the field of catalysis, N,N'-bis(trimethylsilyl)ethylenediamine is used as a ligand to form stable complexes with transition metals, enhancing the efficiency and selectivity of various catalytic processes.
Used in Chemical Research:
N,N'-bis(trimethylsilyl)ethylenediamine is utilized as a research tool to explore new reaction pathways and develop innovative synthetic methods, thanks to its unique structural features and protective capabilities for nitrogen atoms.
Used in Industrial Applications:
In the chemical industry, N,N'-bis(trimethylsilyl)ethylenediamine is employed to improve the synthesis of complex organic molecules and fine chemicals, leveraging its protective and catalytic properties to streamline production processes and increase yields.

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 107-15-3 ethylenediamine 
• 3385-94-2 hexamethyldisilathiane 
• 1450-14-2 1,1,1,2,2,2-hexamethyldisilane 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 

Downstream Products

• 7126-86-5 N,N'-Bis-trimethylsilyl-N-(methyl-diphenyl-silyl)-aethylendiamin 
• 7036-91-1 N,N'-bis-trimethylsilanyl-N-triphenylsilanyl-ethane-1,2-diamine 
• 7166-24-7 N-(dimethyl-phenyl-silanyl)-N,N'-bis-trimethylsilanyl-ethane-1,2-diamine 
• 4403-78-5 ditosylethylenediamine 
• 7036-81-9 2,2-diphenyl-1,3-bis-trimethylsilanyl-[1,3,2]diazasilolidine 
• 7036-80-8 2-methyl-2-phenyl-1,3-bis-trimethylsilanyl-[1,3,2]diazasilolidine 
• 142941-19-3 1,3-Bis(trimethylsilyl)-2--2-<3'',3''-dimethyl-1''-trimethylsilyl-but-1''-enyl>-1,3-diaza-2-silacyclopentan 
• 4392-52-3 N,N'-bis(phenylsulfonyl)ethylenediamine 

Relevant academic research and scientific papers

Thermal decomposition of [Me3SiNCH2CH2NSiMe3] · Li2(THF)2 to [LiN(SiMe3)2 · THF]2 via a 1,4-trimethylsilyl shift

The dilithium salt [Me3SiNCH2CH2NSiMe3] · Li2(THF)2 decomposes slowly upon heating forming a metastable structure of the crystalline [LiN(SiMe3) · THF]2. The crystal s

New cyclic and spirocyclic aminosilanes

New cyclic and spirocyclic aminosilanes were synthesised using ethylenediamine, 2-aminoben-zylamine, 1,8-diaminonaphthalene, o-phenylenediamine, and trans-cyclohexane-1,2-diamine as starting material. These diamines were converted into aminosilanes using

Binuclear tantalum complex and preparation method thereof

The invention relates to a binuclear tantalum complex and a preparation method thereof. The preparation method comprises the steps of: 1) dissolving a diamino compound into an alkane solvent, dropwiseadding trimethylchlorosilane, carrying out stirring, th

Intramolecular catalysis of aminolysis of phosphorus heterocycles incorporating an α-aminoamide moiety. III. Synthesis of 2-oxo or 2-thioxo 1,3-disulfonyl-1,3,2-diazaphospholidines and reactions with amines and alcohols

A series of 2-oxo or 2-thioxo 1,3-disulfonyl-1,3,2-diazaphospholidines 4 was prepared by condensation of phosphonyl dichlorides 2 with bis-N,N′-sulfonylethylenediamines 1 in pyridine. Complete aminolysis or alcoholysis of heterocycles 4 took place with regeneration of sulfonyldiamines 1. These reactions are very sensitive to steric hindrance, and hydrolysis is generally favoured over aminolysis. The results are discussed in terms of mechanisms of phosphorylation.

Silaheterocycles, XVII. Synthesis and Cycloaddition Reactions of Novel Amino Cyclic Silenes

The silene 2 is formed by reacting 2-chloro-1,3-bis(trimethylsilyl)-2-vinyl-1,3-diaza-2-silacyclopentane (5) with LiBut in n-pentane in the temperature range from -10 to + 10 deg C.The reaction primarily leads to the corresponding α-lithio addu