Trimethyl[2-[(trimethylsilyl)methyl]benzyl]ammonium Iodide

Base Information

• Chemical Name: Trimethyl[2-[(trimethylsilyl)methyl]benzyl]ammonium Iodide
• CAS No.: 83781-47-9
• Molecular Formula: C14H26NSi.I
• Molecular Weight: 363.357
• DSSTox Substance ID: DTXSID10476272
• Mol file: 83781-47-9.mol

Synonyms:Trimethyl[2-[(trimethylsilyl)methyl]benzyl]ammonium Iodide;83781-47-9;trimethyl-[[2-(trimethylsilylmethyl)phenyl]methyl]azanium;iodide;trimethyl[2-[(trimethylsilyl)methyl]benzyl]ammoniumiodide;DTXSID10476272;MFCD12407129;AKOS015833270;T2625;T72982;Trimethyl[2-(trimethylsilylmethyl)benzyl]ammonium iodide

Chemical Property of Trimethyl[2-[(trimethylsilyl)methyl]benzyl]ammonium Iodide

Chemical Property:

• PSA: 0.00000
• LogP: 0.58310
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 363.08792
• Heavy Atom Count: 17
• Complexity: 212

Purity/Quality:

98% ^*data from raw suppliers

Trimethyl[2-[(trimethylsilyl)methyl]benzyl]ammonium Iodide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C[N+](C)(C)CC1=CC=CC=C1C[Si](C)(C)C.[I-]

Technology Process of Trimethyl[2-[(trimethylsilyl)methyl]benzyl]ammonium Iodide

There total 2 articles about Trimethyl[2-[(trimethylsilyl)methyl]benzyl]ammonium Iodide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

N,N-dimethyl(2-methylbenzyl)amine (4525-48-8) → trimethyl<2-<(trimethylsilyl)methyl>benzyl>ammonium iodide (83781-47-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) n-BuLi, 2.) Et₃N / 1.) Et₂O, room temperatutre, 22 h, 2.) room temperature, 4 h

2: acetonitrile / 1 h / Heating

With n-butyllithium; triethylamine; In acetonitrile;

DOI:10.1021/ja00390a036

Reference yield:

benzyl>dimethylamine (41839-73-0) + methyl iodide (74-88-4) → trimethyl<2-<(trimethylsilyl)methyl>benzyl>ammonium iodide (83781-47-9)

Guidance literature:

In acetonitrile; for 1h; Yield given; Heating;

DOI:10.1021/ja00390a036

Reference yield: 54.0%

2-buten-4-olide (497-23-4) + trimethyl<2-<(trimethylsilyl)methyl>benzyl>ammonium iodide (83781-47-9) → (3ar,9ac)-3a,4,9,9a-tetrahydro-3H-naphtho[2,3-c]furan-1-one (7463-95-8,7506-70-9)

Guidance literature:

With potassium fluoride; for 5h; Heating;

DOI:10.1016/S0040-4020(00)00126-5

upstream raw materials:

benzyl>dimethylamine

methyl iodide

N,N-dimethyl(2-methylbenzyl)amine

Downstream raw materials:

spiro-(5,5)-2,3-benzo-6-methyleneundeca-7,9-diene

5,6,11,12-tetrahydro-dibenzo[a,e]cyclooctene

1,2-dimethylenebenzene

trimethylsilyl fluoride

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