57186-68-2

Basic information

• Product Name: N-Ethyl-N,4-dimethylbenzenesulfonamide
• Synonyms: N-Ethyl-N,4-dimethylbenzenesulfonamide
• CAS NO: 57186-68-2
• Molecular Formula: C₁₀H₁₅NO₂S
• Molecular Weight: 213.3
• Mol File: 57186-68-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Ethyl-N,4-dimethylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Ethyl-N,4-dimethylbenzenesulfonamide(57186-68-2)
• EPA Substance Registry System: N-Ethyl-N,4-dimethylbenzenesulfonamide(57186-68-2)

Safety Data

• Hazardous Substances Data: 57186-68-2(Hazardous Substances Data)

Upstream product

• 75-03-6 ethyl iodide 
• 640-61-9 N-methyl-p-toluenesulfonylamide 
• 624-78-2 N-Ethylmethylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 4788-37-8 N-ethyl-N-methylbenzylamine 
• 7677-24-9 trimethylsilyl cyanide 
• 16697-83-9 N-methyl-N-tosylacetamide 
• 141-78-6 ethyl acetate 
• 70-55-3 toluene-4-sulfonamide 
• 80-39-7 N-ethyl-4-methyl-benzenesulfonamide 
• 74-88-4 methyl iodide 
• 16181-39-8 O-ethyl N-methyl toluene-4-sulphonimidate 
• 74-96-4 ethyl bromide 
• 5228-66-0 N-Methyl-N--formamid-diaethylacetal 

Relevant articles and documents

Debenzylative Sulfonylation of Tertiary Benzylamines Promoted by Visible Light

An efficient, general, inexpensive, and environmentally friendly photosynthesis of sulfonamides via visible light promoted debenzylative sulfonylation of tertiary benzylamines is described. Compared to the traditional S?N coupling reactions, which are promoted by oxidative C?N bond cleavage of symmetrical tertiary alkylamines, this strategy provides a selective C?N bond cleavage protocol and avoids the use of transition-metal, explosive oxidants, and ligands.

The mechanism of alkene elimination from protonated toluenesulphonamides generated by electrospray ionisation

The positive ion electrospray mass spectra of a range of sulphonamides of general structure CH3C6H4SO2NHR1 [R1 = CnH2n+1 (n = 1-7), CnH2n-1 (n = 3, 4), C6H5, C6H5CH2 and C6H5CH(CH3)] and CH3C6H4SO2NR1R2 [R1, R2 = CnH2n+1 (n = 1-8)] are reported and discussed. The protonated sulphonamides derived from saturated primary and secondary aliphatic amines generally fragment to only a limited extent unless energised by collision. Two general fragmentations are observed: firstly, elimination of an alkene, CnH2n, obtained by hydrogen abstraction from one of the CnH2n+1 alkyl groups on nitrogen; secondly, cleavage to form CH3C6H4SO2+. The mechanism by which an alkene is lost has been probed by studying the variation of the intensity of the [M + H - CnH2n]+ signal with the structure of the alkyl substituent(s) on nitrogen and by monitoring the competition between the loss of different alkenes from protonated unsymmetrical sulphonamides in which two different alkyl groups are attached to nitrogen. This fragmentation is favoured by branching of the alkyl group at the carbon atom directly attached to nitrogen, thus suggesting that it involves a mechanism in which the stability of the cation obtained by stretching the bond connecting the nitrogen atom to the alkyl group is critical. This interpretation also explains the competition between alkene elimination and cleavage to form CH3C6H4SO2+ (and, in some cases, cleavage to form C6H5CH2+ or [C6H5CHCH3]+).

NAlkylation of tosylamides using esters as primary and tertiary alkyl sources: Mediated by hydrosilanes activated by a ruthenium catalyst

Select your group: Either a primary or tertiary alkyl group can be selectively introduced onto the nitrogen atom of tosylamides in a ruthenium-catalyzed reaction employing hydrosilanes through a judicious choice in the esters that serve as the alkyl source (see scheme; Ts= 4-toluenesulfonyl). These N-alkylation reactions are useful for construction of naturally occurring azacyclic skeletons. Copyright