Benzenesulfonamide, 4-methyl-N-(2-methyl-2-propenyl)-N-2-propenyl-

Base Information

• Chemical Name: Benzenesulfonamide, 4-methyl-N-(2-methyl-2-propenyl)-N-2-propenyl-
• CAS No.: 594858-64-7
• Molecular Formula: C14H19NO2S
• Molecular Weight: 265.376
• DSSTox Substance ID: DTXSID50459524
• Nikkaji Number: J1.935.121A
• Wikidata: Q82283307

Synonyms:594858-64-7;Benzenesulfonamide, 4-methyl-N-(2-methyl-2-propenyl)-N-2-propenyl-;Tosyl(2-methylallyl)allylamine;SCHEMBL10017634;DTXSID50459524;SDICGMJIALNGNI-UHFFFAOYSA-N;4-Methyl-N-(2-methylprop-2-en-1-yl)-N-(prop-2-en-1-yl)benzene-1-sulphonamide

Chemical Property of Benzenesulfonamide, 4-methyl-N-(2-methyl-2-propenyl)-N-2-propenyl-

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 265.11365002
• Heavy Atom Count: 18
• Complexity: 387

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)N(CC=C)CC(=C)C

Technology Process of Benzenesulfonamide, 4-methyl-N-(2-methyl-2-propenyl)-N-2-propenyl-

There total 8 articles about Benzenesulfonamide, 4-methyl-N-(2-methyl-2-propenyl)-N-2-propenyl- 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%

4-methyl-N-(2-propenyl)benzenesulfonamide (50487-71-3) + 3-Chloro-2-methylpropene (563-47-3) → N-allyl-4-methyl-N-(2-methylallyl)benzenesulfonamide (594858-64-7)

Guidance literature:

4-methyl-N-(2-propenyl)benzenesulfonamide; With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃;

3-Chloro-2-methylpropene; In N,N-dimethyl-formamide; at 20 ℃; for 12h;

DOI:10.1021/ja037394p

Reference yield: 93.0%

N-(2-methylallyl)-4-toluenesulfonamide (1206-41-3) + allyl bromide (106-95-6) → N-allyl-4-methyl-N-(2-methylallyl)benzenesulfonamide (594858-64-7)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide;

DOI:10.1016/j.tetlet.2003.10.191

Reference yield: 89.0%

2-methyl-3-bromo-1-propene (1458-98-6) + 4-methyl-N-(2-propenyl)benzenesulfonamide (50487-71-3) → N-allyl-4-methyl-N-(2-methylallyl)benzenesulfonamide (594858-64-7)

Guidance literature:

With potassium carbonate; In acetonitrile; Heating;

DOI:10.1002/anie.200454157

upstream raw materials:

N-(2-methylallyl)-4-toluenesulfonamide

allyl bromide

4-methyl-N-(2-propenyl)benzenesulfonamide

3-Chloro-2-methylpropene

Downstream raw materials:

3-methyl-1-[(4-methylphenyl)-sulfonyl]-2,5-dihydro-1H-pyrrole

4-methyl-N-(2-oxo-ethyl)-N-(2-oxo-propyl)-benzenesulfonamide

3-chloromethyl-4,4-dimethyl-1-tosylpyrrolidine

3-chloromethyl-3,4-dimethyl-1-tosylpyrrolidine

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