71827-93-5

Upstream product

• 119513-47-2 5,5,5',5'-tetramethyl-2,2'-(2-methyl-benzylidene)-bis-cyclohexane-1,3-dione 
• 71934-33-3 C₂₄H₃₀O₄ 
• 529-20-4 2-methylphenyl aldehyde 
• 126-81-8 dimedone 

Relevant academic research and scientific papers

Nano-zirconia as an excellent nano support for immobilization of sulfonic acid: A new, efficient and highly recyclable heterogeneous solid acid nanocatalyst for multicomponent reactions

Nano-zirconia-supported sulfonic acid [nano-ZrO2-SO3H (n-ZrSA)] is synthesized by immobilizing sulfonic acid groups on the surface of nano zirconium dioxide to produce a novel heterogeneous reusable solid acid nanocatalyst. This new nanocatalyst is characterized by FT-IR spectroscopy, thermogravimetric analysis (TGA), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), the Hammett acidity function and pH analysis. The introduced nano-zirconia-supported sulfonic acid is used as an efficient and recyclable catalyst for different heterocyclic multicomponent reactions such as the synthesis of hexahydroquinoline, 1,8-dioxo-decahydroacridine, polyhydroquinoline and 1,8-dioxo-octahydroxanthene derivatives. Optimization of the reaction conditions was studied using a central composite design (CCD) which is one of the most widely used response surface methodologies. The newly prepared heterogeneous solid acid nanocatalyst is easily separated and reusable for five cycles without any apparent loss of its catalytic activity, which confirmed the stability of the covalent bonding of the sulfonic acid groups. n-ZrSA has advantages such as its low cost, low toxicity, ease of preparation, good stability, high reusability and operational simplicity.

Nano-WO3-supported sulfonic acid: New, efficient and high reusable heterogeneous nano catalyst

Nano-WO3-supported sulfonic acid [n-WO3-SO3H (n-WSA)] is easily prepared from the reaction of nano WO3 with chlorosulfonic acid as sulfonating agent. This new catalyst is characterized by X-ray diffraction(XRD), field emission scanning electron microscopy (FE-SEM), FT-IR spectroscopy, thermal gravimet-ric analysis (TGA), pH analysis and Hammett acidity function. Nano-WO3-supported sulfonic acid isused as an efficient and recyclable catalyst for some organic reactions such as synthesis of 1,8-dioxo-octahydroxanthene, tetrahydrobenzoxanthene and benzimidazolo quinazolinone derivatives. All of thereactions are very fast and the yields are excellent. The used catalyst was easily separated and reused for 10 runs without appreciable loss of its catalytic activity.

Nano-WO3-supported sulfonic acid: New, efficient and high reusable heterogeneous nano catalyst

Nano-WO3-supported sulfonic acid [n-WO3-SO3H (n-WSA)] is easily prepared from the reaction of nano WO3 with chlorosulfonic acid as sulfonating agent. This new catalyst is characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), FT-IR spectroscopy, thermal gravimetric analysis (TGA), pH analysis and Hammett acidity function. Nano-WO3-supported sulfonic acid is used as an efficient and recyclable catalyst for some organic reactions such as synthesis of 1,8-dioxo-octahydroxanthene, tetrahydrobenzoxanthene and benzimidazolo quinazolinone derivatives. All of the reactions are very fast and the yields are excellent. The used catalyst was easily separated and reused for 10 runs without appreciable loss of its catalytic activity.

A novel polymeric catalyst for the one-pot synthesis of xanthene derivatives under solvent-free conditions

A simple, efficient, and environmentally benign route was developed for the preparation of 14-aryl or alkyl- 14H-dibenzo[a,j]xanthene, 1,8-dioxo- octahydroxanthene and 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-ones from condensation of various aldeh

Magnesium hydrogensulfate [Mg(HSO4)2] as an efficient catalyst for the preparation of silyl ethers, dibenzo[a,j]xanthenes, and octahydroxanthene derivatives

Magnesium hydrogensulfate [Mg(HSO4)2], as a heterogeneous solid acid catalyst, has been used for the mild formation of trimethylsilyl (TMS) ethers from various primary, secondary, and tertiary aliphatic alcohols; aromatic alcohols; a

NMR spectral studies of dimedone-aldehyde adducts Part 2. 1H and 13C NMR studies of the adducts

A detailed study of the 270 MHz 1H and 67 MHz 13C NMR spectra of four series of dimedone adducts and "anhydrides" is presented. A valuable 5JHH homoallylic coupling has been identified which has facilitated sign

CHLOROSULFONATION OF 9-ARYL 3,3,6,6-TETRAMETHYLOCTAHYDROXANTHEN-1,8-DIONES

The 9-aryl-3,3,6,6-tetramethyloctahydroxanthendiones (4-20) react with chlorosulfonic acid to give the sulfonyl chlorides (25, 34, 43, 53, 55, 59, 63, and 65).The xanthendione (7) from m-anisaldehyde afforded the bis-sulfonyl chloride (30).The products we