4141-38-2

Usage

Uses

Used in Chemical Industry:
2,4-diphenyl-1,3-dioxolane is used as a solvent for various chemical processes due to its ability to dissolve a wide range of substances, facilitating reactions and improving the efficiency of industrial operations.
Used in Perfumery:
In the perfume industry, 2,4-diphenyl-1,3-dioxolane is used as a carrier for fragrances, helping to stabilize and prolong the scent of perfumes and other fragranced products.
Used in Pharmaceutical Industry:
2,4-diphenyl-1,3-dioxolane is utilized in the manufacturing of pharmaceuticals, where it serves as a solvent or intermediate in the synthesis of various medicinal compounds.
Used in Organic Synthesis:
2,4-diphenyl-1,3-dioxolane is employed as a reagent or intermediate in the synthesis of other organic compounds, contributing to the development of new materials and chemical products.

Upstream product

• 96-09-3 styrene oxide 
• 100-52-7 benzaldehyde 
• 3162-96-7 methyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 93-56-1 phenylethane 1,2-diol 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 936-51-6 2-phenyl-1,3-dioxolane 
• 2568-25-4 4-methyl-2-phenyl-1,3-dioxolane 
• 772-01-0 2-phenyl-1,3-dioxane 

Downstream Products

• 115061-56-8 O-benzoylmandelic acid 
• 18600-43-6 (2-hydroxy-2-phenylethyl)triphenylphosphonium bromide 
• 100-52-7 benzaldehyde 
• 70959-98-7 2-(benzyloxy)-2-phenylethan-1-ol 
• 838-66-4 2-O-benzyl-1-phenylethane-1,2-diol 
• 10335-95-2 2-hydroxy-2-phenylethyl benzoate 
• 53574-78-0 2-hydroxy-1-phenylethyl benzoate 

Relevant academic research and scientific papers

Iron oxide-pillared clay catalyzed the synthesis of acetonides from epoxides

FeOx-pillared clays (FeOx-pillared bentonite, FeOx-pillared hectorite and FeOx-pillared taeniolite) were synthesized by the intercalation of FeCl3 into clay interlayers and calcination. The synthesize

Iron oxide-pillared clay catalyzed the synthesis of acetonides from epoxides

FeOx-pillared clays (FeOx-pillared bentonite, FeOx-pillared hectorite and FeOx-pillared taeniolite) were synthesized by the intercalation of FeCl3 into clay interlayers and calcination. The synthesize

Phosphonium salts and aldehydes from the convenient, anhydrous reaction of aryl acetals and triphenylphosphine hydrobromide

The reactions of aryl acetals/ketals and triphenylphosphine hydrobromide gave the corresponding aldehydes/ketones and alkyl phosphonium bromides. This reaction was applied to convert acetals/ketals to the corresponding aldehydes/ketones under an anhydrous

Cu(OTf)2-catalyzed selective opening of aryl and vinyl epoxides with carbonyl compounds to give 1,3-dioxolanes

Copper(II) triflate catalyzes the ring-opening of aryl- and vinyl-substituted epoxides with various carbonyl compounds to furnish 1,3-dioxolanes under mild conditions. Alkyl- and alkoxycarbonyl-substituted epoxides remain unchanged under reaction conditio

Stereoelectronic effects in the DIBAL reduction of aryl-1,2-ethanediol benzylidene acetals

Reduction of benzylidene acetal 8 with DIBAL-H selectively gave 4 in 89% yield. 1-Aryl-1,2-diol benzylidene acetals display unusual regioselectivity with electron withdrawing groups on the aryl group.

Transacetalation: a convenient, nonaqueous method for effecting the deprotection of isopropylidene and benzylidene derivatives of sugars

Sugar isopropylidene and benzylidene derivatives can be readily deprotected under nonaqueous conditions by treatment of a dichloromethane solution of the protected sugar with an excess of a sacrificial glycol in the presence of a catalytic amount of p-toluenesulfonic acid.The reaction is conveniently monitored by GLC, and the fully or partially deprotected product precipitates from solution.

N-Benzyl Pyridinium Salta as New Useful Catalysts for Transformation of Epoxides to Cyclic Acetals, Orthoesters, and Orthocarbonates

In the presence of catalytic amount of N-(4-methoxybenzyl)-2-cyanopyridinium hexafluoroantimonate, the reaction of a few epoxides with aldehydes, ketones, lactones, and carbonates efficiently afforded corresponding cyclic acetals, orthoesters, and orthocarbonates under mild conditions.