26271-50-1

Usage

Uses

Used in Organic Synthesis:
1,3-Dichloroacetone Ethylene Ketal is used as a synthetic intermediate for the production of various organic compounds. Its chemical properties, such as being a clear liquid, make it suitable for use in a wide range of chemical reactions, allowing for the creation of diverse molecules with different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,3-Dichloroacetone Ethylene Ketal is used as a key component in the synthesis of certain drugs. Its ability to participate in various chemical reactions enables the development of new medications with potential therapeutic benefits.
Used in Chemical Research:
1,3-Dichloroacetone Ethylene Ketal is also utilized in chemical research as a tool to study the properties and behavior of different compounds. Its clear liquid form allows researchers to observe and analyze its interactions with other substances, leading to a better understanding of chemical reactions and the development of new compounds.
Used in Environmental Applications:
1,3-Dichloroacetone Ethylene Ketal can be employed in environmental applications, such as the treatment of pollutants or the development of eco-friendly materials. Its versatility in organic synthesis makes it a valuable asset in creating solutions to environmental challenges.

InChI:InChI=1/C5H8Cl2O2/c6-3-5(4-7)8-1-2-9-5/h1-4H2

Upstream product

• 107-21-1 ethylene glycol 
• 534-07-6 1,3-Dichloroacetone 

Relevant academic research and scientific papers

Synthesis method of 3-oxetanone

The invention discloses a synthesis method of 3-oxetanone. Specifically, 1, 3-dichloroacetone and ethylene glycol are taken as raw materials, 3-oxetanone is synthesized at high yield through three steps of carbonyl protection reaction, ring closing reaction and deprotection reaction. The preparation method of 3-oxetanone is a synthesis method which is high in yield, low in cost, environment-friendly, easy to operate and suitable for industrialization.

Method for preparing 1,3-dihydroxyacetone from 1,3-dichloroacetone

The invention discloses a method for preparing 1,3-dihydroxyacetone from 1,3-dihydroxyacetone. The method comprises the following steps: by taking 1,3-dichloroacetone and ethylene glycol as raw materials and taking p-toluenesulfonic acid as a catalyst, reacting at the temperature of 0-110 DEG C so as to produce 1,3-dichloroacetone ethylene ketal; adding sodium hydroxide of a certain mass fraction, and hydrolyzing under alkaline conditions so as to obtain 1,3-dihydroxyacetone ethylene ketal; and finally, adding sulfuric acid for acidifying so as to enable the solution to be acidic, obtaining a mixture containing dihydroxyacetone and ethylene glycol, desalting the mixture, evaporating, concentrating, recrystallizing, and filtering, thereby obtaining the dihydroxyacetone crystal, wherein the filtrate is a mixed solution containing sodium sulfate, and the yield of the dihydroxyacetone can reach 60% or higher. The method disclosed by the invention can be used for an industrial production path of dihydroxyacetone, and has the advantages of high yield, low cost, simplicity in operation and separation and the like compared with a biological method, and is convenient for industrial production.

Electrosynthesis of cyclopropanone adducts

Electroreduction of α, α'-dihalo ketones to cyclopropanones (isolated as the hemiacetals or hemiacylals) is accomplished with good yields only with highly alkylated α, α'-dihalo ketones.Attempts to prepare little substituted or unsubstituted cyclopropanon