215813-64-2

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 75-05-8 acetonitrile 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 123-11-5 4-methoxy-benzaldehyde 
• 75-36-5 acetyl chloride 
• 215813-47-1 (E/Z)-2-[2-(4-methoxyphenyl)-1,3-dithiolan-2-yl]-1-(4-methoxyphenyl)ethanone O-methyloxime 
• 215813-60-8 1-(4-Methoxy-phenyl)-2-[2-(4-methoxy-phenyl)-[1,3]dithian-2-yl]-ethylamine 
• 215813-58-4 1-(4-Methoxy-phenyl)-2-[2-(4-methoxy-phenyl)-[1,3]dithiolan-2-yl]-ethylamine 
• 215813-57-3 1-(4-Methoxy-phenyl)-2-[2-(4-methoxy-phenyl)-[1,3]dioxolan-2-yl]-ethylamine 
• 215813-35-7 2-[2-(4-methoxyphenyl)-1,3-dithiolan-2-yl]-1-(4-methoxyphenyl)ethanone 
• 65418-71-5 1,3-bis-(4-methoxyphenyl)-2-ethynyl-1-one 
• 215813-63-1 N-{2-[2-(4-methoxyphenyl)-1,3-dithian-2-yl]-1-(4-methoxyphenyl)ethyl}acetamide 
• 215813-62-0 N-{2-[2-(4-methoxyphenyl)-1,3-dithiolan-2-yl]-1-(4-methoxyphenyl)ethyl}acetamide 
• 215813-61-9 N-{2-[2-(4-methoxyphenyl)-1,3-dioxolan-2-yl]-1-(4-methoxyphenyl)ethyl}acetamide 

Relevant academic research and scientific papers

Nano-sphere silica sulfuric acid: Novel and efficient catalyst in the one-pot multi-component synthesis

In this report, synthesis, characterization and application of nano-sphere silica sulfuric acid as a novel and heterogeneous catalyst for the synthesis of β-acetamido ketone derivatives at room temperature are described. The catalyst has been identified u

Pyrazinium di(hydrogen sulfate) as a novel, highly efficient and homogeneous catalyst for the condensation of enolizable ketones with aldehydes, acetonitrile and acetyl chloride

A highly efficient protocol for the synthesis of β-acetamido ketone or ester derivatives in the presence of pyrazinium di(hydrogen sulfate) {Py(OSO3H)2} as a novel, green and homogeneous solid acid catalyst at room temperature is des

Ionic liquid 3-methyl-1-sulphonic acid imidazolium chloride {[Msim]Cl}: A highly efficient, mild and green catalyst for the synthesis of β-acetamido ketones

Bronstedacidic ionic liquid 3-methyl-1-sulphonic acid imidazolium chloride {[Msim]Cl} is utilized as a highly efficient, inexpensive, mild and green catalyst for the synthesis of β-acetamido ketones by the one-pot multi-component coupling between acetophenones, arylaldehydes, acetonitrile and acetyl chloride at roomtemperature. Under these conditions, the title compounds are produced in high to excellent yields and in relatively short reaction times. In addition, this method is superior to reported methods, for the synthesis of β-acetamido ketones and is applicable for the synthesis of tris(β-acetamido ketone).

Ionic liquid triethylamine-bonded sulfonic acid {[Et3N-SO 3H]Cl} as a novel, highly efficient and homogeneous catalyst for the synthesis of β-acetamido ketones, 1,8-dioxo-octahydroxanthenes and 14-aryl-14H-dibenzo[a,j]xanthenes

In this work, the efficiency, generality and applicability of novel Br?nsted acidic ionic liquid triethylamine-bonded sulfonic acid {[Et 3N-SO3H]Cl, N,N-diethyl-N-sulfoethanammonium chloride} as homogeneous and green catalyst for org

Efficient synthesis of β-acetamido ketones and esters using aluminum chloride as an inexpensive and green catalyst

Aluminum chloride (AlCl3) efficiently catalyzes one-pot multicomponent condensation of enolizable ketones or alkyl acetoacetates with aldehydes, acetonitrile and acetyl chloride to afford β-acetamido ketone or ester derivatives in high to excel

Solid-supported sulfonic acid-containing catalysts efficiently promoted one-pot multi-component synthesis of β-acetamido carbonyl compounds

Silica-functionalized sulfonic acid (SFSA) and sulfuric acid-modified polyethylene glycol-6000 (PEG-OSO3H) efficiently catalysed one-pot multi-component condensation of enolizable ketones or alkyl acetoacetates with arylaldehydes, acetonitrile

An efficient and simple one-pot synthesis of β-acetamido ketones catalyzed by ytterbium triflate in ionic liquid

Ytterbium triflate immobilized in the ionic liquid [bmim][BF4] catalyzes the three-component coupling of aromatic aldehydes, enolizable ketones, and acetonitrile in the presence of acetyl chloride at room temperature to afford -acetamido ketones in good yields. The catalyst can be recovered and recycled for subsequent reactions without any appreciable loss of efficiency.

1,3-Diphenylpropane-1,3-diamines XII [1]. A novel approach to stereodefined oximes and oxime ethers of monothioketalized 1,3-diketones and their conversion to 3-aminooximes

Mono-O,O-and mono-S,S-ketals of 1,3-diphenylpropane-1,3-diones react with hydroxylamine hydrochloride and O-methylhydroxylamine hydrochloride affording mixtures of (E/Z) isomers which are hard to separate or are even unseparable. Isomerically pure oximes