136932-93-9

Basic information

• Product Name: Benzene, 1-[(2,3-dibromopropyl)sulfonyl]-4-methyl-
• CAS NO: 136932-93-9
• Molecular Formula: C10H12Br2O2S
• Molecular Weight: 356.078
• Mol File: 136932-93-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1-[(2,3-dibromopropyl)sulfonyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-[(2,3-dibromopropyl)sulfonyl]-4-methyl-(136932-93-9)
• EPA Substance Registry System: Benzene, 1-[(2,3-dibromopropyl)sulfonyl]-4-methyl-(136932-93-9)

Safety Data

• Hazardous Substances Data: 136932-93-9(Hazardous Substances Data)

Upstream product

• 3112-87-6 1-methyl-4-(prop-2-ene-1-sulfonyl)benzene 
• 824-79-3 sodium 4-methylbenzenesulfinate 

Downstream Products

• 727385-71-9 7-amino-3-(4-methylphenylsulfonylmethyl)-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one 
• 32353-96-1 (E)-4,4'-(prop-1-ene-1,3-diyldisulfonyl)bis(methylbenzene) 
• 103038-44-4 3-bromo-1-(p-tolylsulfonyl)propene 

Relevant articles and documents

Isomerisation of Vinyl Sulfones for the Stereoselective Synthesis of Vinyl Azides

Reported is the construction, and facile base-mediated conversation of ten differently substituted 3-azido E-vinyl sulfones (γ-azido-α,β-unsaturated sulfones) into their isomeric vinyl azide counterparts. The requisite 3-azido E-vinyl sulfones were prepared from 3-bromo E-vinyl sulfones, which in turn were accessed from allyl sulfones via a bromination-elimination sequence. In relation to this a one-pot azidation-isomerisation sequence was developed which enabled the direct formation of the vinyl azides from the corresponding 3-bromo E-vinyl sulfones. Similarly, a convenient one-pot Horner–Wadsworth–Emmons olefination-isomerisation approach was utilised in order to prepare some of the allylic sulfones used in this study. The vinyl azide forming process typically proceeded with high levels of Z-selectivity, although this was dependent on the vinyl sulfone substitution pattern. Thus, with either no substituent or a methyl group in the γ- or β-position, relative to the sulfone, good, to high levels of Z-selectivity (Z/E = 85:15 to ≥ 95:5) were obtained. However, incorporation of an α-sulfonyl methyl substituent led to an E-selective process (Z/E = 20:80). A non-bonding interaction between the azido group and the α-sulfonyl vinylic proton is proposed, which acts as a conformational control mechanism to help guide the stereochemical outcome.

One-Pot Allylation-Intramolecular Vinylogous Michael Addition-Isomerization Cascade of o-Hydroxycinnamates and Congeners: Synthesis of Substituted Benzofuran Derivatives

A unique intramolecular vinylogous Michael addition leading to the synthesis of heterocycles has been disclosed. Base-promoted one-pot sequential O-allylation of o-hydroxy-cinnamates or -cinnamonitrile or -chalcones with γ-bromocrotonates followed by an intramolecular conjugate addition of vinylogous Michael donors resulted in the formation of highly substituted benzofuran derivatives in good to excellent yields. The intramolecular event followed by two [1,3]-H shifts leading to aromatization appears to be the key to the success of this unprecedented transformation.

Direct N-H/α,α,β,β-C(sp3)-H functionalization of piperidine via an azomethine ylide route: synthesis of spirooxindoles bearing 3-substituted oxindoles

A protocol for the direct functionalization of N-H/α,α,β,β-C(sp3)-H of piperidine without any metal or external oxidants is reported. This reaction is promoted by 4-(trifluoromethyl)benzoic acid via an azomethine ylide intermediate. This is a simple method for the synthesis of spirooxindoles bearing 3-substituted oxindole moieties.