Aziridine, 2,2,3,3-tetramethyl-1-[(4-methylphenyl)sulfonyl]-

Base Information

• Chemical Name: Aziridine, 2,2,3,3-tetramethyl-1-[(4-methylphenyl)sulfonyl]-
• CAS No.: 432545-79-4
• Molecular Formula: C13H19NO2S
• Molecular Weight: 253.365
• DSSTox Substance ID: DTXSID30476219
• Nikkaji Number: J1.595.461B
• Wikidata: Q82307252
• Mol file: 432545-79-4.mol

Synonyms:432545-79-4;Aziridine, 2,2,3,3-tetramethyl-1-[(4-methylphenyl)sulfonyl]-;DTXSID30476219

Chemical Property of Aziridine, 2,2,3,3-tetramethyl-1-[(4-methylphenyl)sulfonyl]-

Chemical Property:

• XLogP3: 2.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 253.11365002
• Heavy Atom Count: 17
• Complexity: 384

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)S(=O)(=O)N2C(C2(C)C)(C)C

Technology Process of Aziridine, 2,2,3,3-tetramethyl-1-[(4-methylphenyl)sulfonyl]-

There total 2 articles about Aziridine, 2,2,3,3-tetramethyl-1-[(4-methylphenyl)sulfonyl]- 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: 98.0%

2,3-Dimethyl-2-butene (563-79-1) + [N-(p-tolylsulfonyl)imino]phenyliodinane (55962-05-5) → 2,2,3,3-tetramethyl-1-tosylaziridine (432545-79-4)

Guidance literature:

With C₁₇H₁₃ClCuN₃O₂; sodium tetrakis[(3,5-di-trifluoromethyl)phenyl]borate; In dichloromethane; at 0 - 22 ℃; Inert atmosphere;

DOI:10.1021/acs.inorgchem.9b02618

Reference yield:

2,3-Dimethyl-2-butene (563-79-1) → 2,2,3,3-tetramethyl-1-tosylaziridine (432545-79-4)

Guidance literature:

With NH-pyrazole; In dichloromethane; at 24.85 ℃; Kinetics;

DOI:10.1021/ja9913481

Reference yield: 70.0%

2,2,3,3-tetramethyl-1-tosylaziridine (432545-79-4) → N-(2-fluoro-1,1,2-trimethyl-propyl)-4-methyl-benzenesulfonamide + 4-methyl-N-(1,1,2-trimethyl-allyl)-benzenesulfonamide

Guidance literature:

With boron trifluoride diethyl etherate; In chloroform; at -18 ℃;

DOI:10.1039/b109445a

upstream raw materials:

2,3-Dimethyl-2-butene

[N-(p-tolylsulfonyl)imino]phenyliodinane

Downstream raw materials:

N-(1,2,2-trimethylpropylidine)-p-toluenesulfonamide

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