24991-47-7

Usage

Chemical Properties

white powder

Upstream product

• 64-17-5 ethanol 
• 141-52-6 sodium ethanolate 
• 17277-94-0 (4-chloro-phenethyl)-dimethyl sulfonium ; bromide 
• 1615-02-7 3-(4-chlorophenyl)prop-2-enoic acid 
• 108-24-7 acetic anhydride 
• 104-88-1 4-chlorobenzaldehyde 
• 917-64-6 methyl magnesium iodide 
• 6068-86-6 (2-(p-Chlorophenyl)ethyl)trimethylammonium bromide 
• 106-39-8 bromochlorobenzene 
• 74-85-1 ethene 
• 637-87-6 1-Chloro-4-iodobenzene 
• 754-06-3 vinyltrimethyltin 
• 1826-67-1 vinyl magnesium bromide 
• 6529-53-9 1-(2-bromoethyl)-4-chlorobenzene 

Downstream Products

• 511533-74-7 1-(1-bromo-3,3,3-trichloro-propyl)-4-chloro-benzene 
• 1009-43-4 4-(trimethylsilyl)styrene 
• 70263-54-6 [5-(4-chloro-phenyl)-2-phenyl-isoxazolidin-3-yl]-phenyl-methanone 
• 1824-55-1 6-chloro-3-(4-chloro-benzyl)-1,1-dioxo-1,2,3,4-tetrahydro-1λ⁶-benzo[1,2,4]thiadiazine-7-sulfonic acid amide 
• 91647-69-7 Diaethoxy-<4-vinyl-phenyl>-phosphin 
• 1550-92-1 3-(4-chloro-benzyl)-1,1-dioxo-6-trifluoromethyl-1,2,3,4-tetrahydro-1λ⁶-benzo[1,2,4]thiadiazine-7-sulfonic acid amide 
• 51954-36-0 1-Chloro-4-(2,2-diiodo-cyclopropyl)-benzene 
• 70372-39-3 1-chloro-4-(1,2-dithiocyanatoethyl)benzene 
• 70372-43-9 1-Chloro-4-(1-isothiocyanato-2-thiocyanato-ethyl)-benzene 
• 39791-82-7 5-(4-chloro-phenyl)-2-[1-(4-chloro-phenyl)-2-nitro-ethoxy]-3,3-dinitro-isoxazolidine 
• 51779-45-4 1-(4-Chloro-phenyl)-spiro[2.4]hepta-4,6-diene 
• 14331-43-2 6-bromo-3-(4-chloro-benzyl)-1,1-dioxo-1,2,3,4-tetrahydro-1λ⁶-benzo[1,2,4]thiadiazine-7-sulfonic acid amide 
• 54836-54-3 2-(4-chlorophenyl)cyclopropanone dimethyl acetal 
• 57765-59-0 2-(p-Chlorophenyl)isopropylidenecyclopropane 

Relevant academic research and scientific papers

Photoredox Catalyzed Sulfonylation of Multisubstituted Allenes with Ru(bpy)3Cl2 or Rhodamine B

A highly regio- and stereoselective sulfonylation of allenes was developed that provided direct access to α, β-substituted unsaturated sulfone. By means of visible-light photoredox catalysis, the free radicals produced by p-toluenesulfonic acid reacted with multisubstituted allenes to obtain Markovnikov-type vinyl sulfones with Ru(bpy)3Cl2 or Rhodamine B as photocatalyst. The yield of this reaction could reach up to 91%. A series of unsaturated sulfones would be used for further transformation to some valuable compounds.

Mild and efficient desulfurization of thiiranes with MoCl5/Zn system

Desulfurization of a variety of thiiranes to alkenes occurs chemoselectively in high yields upon treatment with MoCl5/Zn system under mild conditions. The new methodology demonstrates high functional group tolerance toward chloro, bromo, fluoro, methoxy, ester, ether and keto groups.

Vinyl Thianthrenium Tetrafluoroborate: A Practical and Versatile Vinylating Reagent Made from Ethylene

The use of vinyl electrophiles in synthesis has been hampered by the lack of access to a suitable reagent that is practical and of appropriate reactivity. In this work we introduce a vinyl thianthrenium salt as an effective vinylating reagent. The bench-stable, crystalline reagent can be readily prepared from ethylene gas at atmospheric pressure in one step and is broadly useful in the annulation chemistry of (hetero)cycles, N-vinylation of heterocyclic compounds, and palladium-catalyzed cross-coupling reactions. The structural features of the thianthrene core enable a distinct synthesis and reactivity profile, unprecedented for other vinyl sulfonium derivatives.

Water-hydrogen-supplying iridium catalytic alkyne semi-reduction selective synthesis method Process for trans-olefines

The method comprises the following steps: DPPE, COD, a catalyst, water and alkyne are subjected to reduction reaction of alkyne in an organic solvent, and cis-olefin is generated by reaction under nitrogen protection. The ligand DPPE, the catalyst, the water and the alkyne are subjected to a reduction reaction of alkyne in an organic solvent, and a trans-olefin is generated by the reaction under nitrogen protection. The reactor for the reduction reaction is a sealed pressure-resistant reactor, the temperature of the reduction reaction is 100 - 130 °C, and the reduction reaction time is 20 - 48h. The amount of the catalyst used is 5 - 20% of the molar amount of alkyne, and the amount of water is 10 - 50 times of the molar amount of alkyne. The ligand is used in an amount 0.2 - 5 times the molar amount of catalyst. The catalyst system disclosed by the invention has extremely high chemical reaction and stereoselectivity, and cis or trans olefinic products can be synthesized at high yield. The catalytic system has strong universality on substrates, and alkynes containing various functional groups can efficiently carry out high-selectivity reduction reaction.

Zinc salt-catalyzed reduction of α-aryl imino esters, diketones and phenylacetylenes with water as hydrogen source

The zinc salt-catalyzed reduction of α-aryl imino esters, diketones and phenylacetylenes with water as hydrogen source and zinc as reductant was successfully conducted. The presented method provides a low-cost, environmentally friendly and practical preparation of α-aryl amino esters, α-hydroxyketones and phenylethylenes. By using D2O as deuterium source, the corresponding products were obtained in high efficiency with excellent deuterium incorporation rate, which gives a cheap and safe tool for access to valuable deuterium-labelled compounds. This journal is

Indene formation upon borane-induced cyclization of arylallenes, 1,1-carboboration, and retro-hydroboration

We herein report the reaction of arylallenes with tris(pentafluorophenyl)borane that yields pentafluorophenyl substituted indenes. The tris(pentafluorophenyl)borane induces the cyclization of the allene and transfers a pentafluorophenyl ring in the course of this reaction. A Hammett plot analysis and DFT computations indicate a 1,1-carboboration to be the C-C bond-forming step.

Copper-Catalyzed Sulfonylation of Cyclobutanone Oxime Esters with Sulfonyl Hydrazides

A copper-catalyzed radical cross-coupling of cyclobutanone oxime esters with sulfonyl hydrazides has been developed. The copper-based catalytic system proved crucial for cleavage of the C-C bond of cyclobutanone oximes and for selective C-S bond-formation involving persistent sulfonyl-metal radical intermediates. This protocol is distinguished by the low-cost catalytic system, which does not require ligand, base, or toxic cyanide salt, and by the use of readily accessible starting materials, as well as broad substrate scope, providing an efficient approach to various diversely substituted cyano-containing sulfones.

Electrochemistry enabled selective vicinal fluorosulfenylation and fluorosulfoxidation of alkenes

Both sulfur and fluorine play important roles in organic synthesis, the life science, and materials science. The direct incorporation of these elements into organic scaffolds with precise control of the oxidation states of sulfur moieties is of great significance. Herein, we report the highly selective electrochemical vicinal fluorosulfenylation and fluorosulfoxidation reactions of alkenes, which were enabled by the unique ability of electrochemistry to dial in the potentials on demand. Preliminary mechanistic investigations revealed that the fluorosulfenylation reaction proceeded through a radical-polar crossover mechanism involving a key episulfonium ion intermediate. Subsequent electrochemical oxidation of fluorosulfides to fluorosulfoxides were readily achieved under a higher applied potential with the adventitious H2O in the reaction mixture.

Base-Mediated Site-Selective Hydroamination of Alkenes

We present a base-mediated hydroamination protocol, using substoichiometric amounts of a hydrosilane and potassium tertbutoxide, that operates under mild conditions at 30 °C. Many aryl- and heteroatom-substituted olefins as well as arylamines are tolerated, affording the desired products with complete regioselectivity. Preliminary mechanistic investigations reveal a non-radical pathway for hydroamination. A sequential remote hydroamination strategy involving an initial Fe-catalysed olefin isomerisation followed by our base-mediated hydroamination was also developed to directly access-arylamines from terminal aliphatic alkenes.

Polymerization of Allenes by Using an Iron(II) β-Diketiminate Pre-Catalyst to Generate High Mn Polymers

Herein, we report an iron(II)-catalyzed polymerization of arylallenes. This reaction proceeds rapidly at room temperature in the presence of a hydride co-catalyst to generate polymers of weight up to Mn=189 000 Da. We have determined the polymer structure and chain length for a range of monomers through a combination of NMR, differential scanning calorimetry (DSC) and gel permeation chromatography (GPC) analysis. Mechanistically, we postulate that the co-catalyst does not react to form an iron(II) hydride in situ, but instead the chain growth is proceeding via a reactive Fe(III) species. We have also performed kinetic and isotopic experiments to further our understanding. The formation of a highly unusual 1,3-substituted cyclobutane side-product is also investigated.