Benzenesulfonamide, 4-methyl-N-(1-methyl-1-phenylethyl)-

Base Information

• Chemical Name: Benzenesulfonamide, 4-methyl-N-(1-methyl-1-phenylethyl)-
• CAS No.: 66898-03-1
• Molecular Formula: C16H19NO2S
• Molecular Weight: 289.398
• DSSTox Substance ID: DTXSID00397008
• Nikkaji Number: J1.205.868C

Synonyms:66898-03-1;Benzenesulfonamide, 4-methyl-N-(1-methyl-1-phenylethyl)-;SCHEMBL18726029;DTXSID00397008;AB00018784-01;N-(alpha,alpha-Dimethylbenzyl)-p-toluenesulfonamide

Chemical Property of Benzenesulfonamide, 4-methyl-N-(1-methyl-1-phenylethyl)-

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 289.11365002
• Heavy Atom Count: 20
• Complexity: 397

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of Benzenesulfonamide, 4-methyl-N-(1-methyl-1-phenylethyl)-

There total 26 articles about Benzenesulfonamide, 4-methyl-N-(1-methyl-1-phenylethyl)- 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: 99.0%

α,α-dimethylbenzyl 2-methylpropanoate (7774-60-9) + toluene-4-sulfonamide (70-55-3) → N-(α,α-dimethylbenzyl)-p-toluenesulfonamide (66898-03-1)

Guidance literature:

With dimethylethylsilane; (Ace)Ru₃(CO)7; In dichloromethane; at 20 ℃; for 6h; Inert atmosphere;

DOI:10.1002/anie.201201426

Reference yield: 95.0%

p-toluenesulfonyl chloride (98-59-9) + 2-phenyl-2-propylamine (585-32-0) → N-(α,α-dimethylbenzyl)-p-toluenesulfonamide (66898-03-1)

Guidance literature:

With triethylamine; In dichloromethane; at 0 ℃;

DOI:10.1021/jo062385v

Reference yield: 80.0%

Isopropylbenzene (98-82-8) + [N-(p-tolylsulfonyl)imino]phenyliodinane (55962-05-5) → N-(α,α-dimethylbenzyl)-p-toluenesulfonamide (66898-03-1)

Guidance literature:

[Ru(Me₃tacn)(CF₃CO₂)3]; In acetonitrile; at 25 ℃; for 3h;

DOI:10.1021/jo000881s

upstream raw materials:

p-toluenesulfonyl chloride

2-phenyl-2-propylamine

Isopropylbenzene

sodium p-toluenesulfonamide

Downstream raw materials:

N-Allyl-4-methyl-N-(1-methyl-1-phenyl-ethyl)-benzenesulfonamide

2-iodo-4-methyl-N-(2-phenylpropan-2-yl)benzenesulfonamide

4-methyl-2-phenyl-N-(2-phenylpropan-2-yl)benzenesulfonamide

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