75230-41-0

Usage

Uses

Used in Pharmaceutical Industry:
4'-(2-ACETOXYETHOXY)ACETOPHENONE is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Fragrance Industry:
In the fragrance industry, 4'-(2-ACETOXYETHOXY)ACETOPHENONE is used as a key component in the creation of various scent profiles. Its ability to react with other compounds contributes to the formation of unique and complex aromas.
Used as a Chemical Intermediate in Organic Synthesis:
4'-(2-ACETOXYETHOXY)ACETOPHENONE is utilized as a chemical intermediate in the synthesis of a wide range of organic compounds. Its reactivity and functional groups make it a valuable building block for the development of new materials and products in various industries.

Upstream product

• 6192-44-5 2-phenoxyethyl acetate 
• 64-19-7 acetic acid 
• 31769-45-6 1-(4-(2-hydroxyethoxy)phenyl)ethanone 
• 75-36-5 acetyl chloride 

Downstream Products

• 31769-45-6 1-(4-(2-hydroxyethoxy)phenyl)ethanone 

Relevant academic research and scientific papers

Chemoselective and ligand-free aerobic oxidation of benzylic alcohols to carbonyl compounds using alumina-supported mesoporous nickel nanoparticle as an efficient recyclable heterogeneous catalyst

An economically efficient and operationally simple ligand-free protocol for the chemoselective oxidation of benzylic alcohols to carbonyl compounds has been developed using alumina-supported nickel nanoparticles as a stable recyclable heterogeneous catalyst along with potassium tert-butoxide in the presence of aerial oxygen as an eco-friendly oxidant. The aliphatic alcohols remained unaffected under the present condition. Excellent chemoselectivity has also been demonstrated through intermolecular and intramolecular competition experiments. This protocol accommodates a diverse range of substituents with the tolerance of various sensitive moieties during the reaction. The catalyst could be recovered by filtration and reused consecutively without any significant loss in the catalytic activity. Moreover, the heterogeneity of the catalyst has also been established by the “hot filtration method (Sheldon's test)”.

SYNTHESIS OF ACYL 1-ACETOXY-2-PHENOXYETHANES AND THE CORRESPONDING HYDROXY DERIVATIVES

Acyl 1-acetoxy-2-phenoxyethanes Ia-Id were prepared by aluminium chloride or polyphosphoric acid-catalyzed Friedel-Crafts acylation.Subsequent hydrolysis gave the corresponding alcohols IIa-IId.The formation of ortho-isomers during acylation was not observed.