688-29-9

Usage

Uses

Used in Chemical Industry:
3,3-diethoxy-1,1,1-trifluoropropane is used as a solvent for various industrial applications, providing a medium for chemical reactions to occur and facilitating the process of dissolving substances.
Used in Organic Synthesis:
In the field of organic synthesis, 3,3-diethoxy-1,1,1-trifluoropropane serves as a reagent, contributing to the formation of new chemical compounds and aiding in the synthesis of complex organic molecules.
Used in Aerosol Products:
3,3-diethoxy-1,1,1-trifluoropropane is utilized as a propellant in aerosol products, enabling the efficient dispersion of substances in a fine mist or spray form, which is crucial for applications such as personal care, household, and industrial products.
Safety Measures:
Due to its flammable nature, 3,3-diethoxy-1,1,1-trifluoropropane requires careful handling to prevent fire or explosion hazards. Additionally, it is essential to implement proper safety measures to avoid harmful effects from inhalation, ingestion, or skin contact, ensuring the well-being of individuals working with this chemical.

Upstream product

• 64-17-5 ethanol 
• 126015-28-9 (Z)-1-ethoxy-3,3,3-trifluoroprop-1-ene 
• 677-21-4 1,1,1-trifluoropropylene 
• 126015-38-1 1-ethoxy-3,3,3-trifluoro-1-propene 
• 122372-43-4 2-(2,2,2-trifluoroethyl)-1,3-dithiane 
• 754-12-1 2,3,3,3-tetrafluoro-propene 

Downstream Products

• 460-40-2 3,3,3-trifluoropropanal 
• 201861-97-4 1,1-Bisbenzylthio-3,3,3-trifluoropropane 

Relevant academic research and scientific papers

Atom-economical synthesis of 3,3,3-trifluoropropanal dialkyl acetals through Pd/C catalyzed acetalization of 3,3,3-trifluoropropene

A facile and efficient procedure for one-step synthesis of 3,3,3-trifluoropropanal dialkyl acetals from readily available 3,3,3-trifluoropropene (TFP) has been developed. The catalyst can be recycled for 4 times without obvious deactivation. This process provides a novel and atom-economical synthetic strategy for the preparation of functional CF3-containing compounds.

Alternative synthetic routes to hydrofluoroolefins

A series of hydrofluoroolefins with -CF=CH2, -CH=CHF and -CH=CF2 groups were designed and prepared via various synthetic routes, including HX or BrF elimination, Wittig-type olefination or fluorination using SF4.

A novel and convenient synthesis of (Z)-3,3,3-trifluoropropenyl alkyl ethers and CF3-substituted propyl acetals as versatile CF3-containing building blocks

A novel and convenient preparation of (Z)-3,3,3-trifluoropropyl alkyl ethers and their further transformation into CF3-substituted propyl acetals is described.

2-(2,2,2-Trifluoroethylidene)-1,3-dithianes. New Intermediates for the Preparation of CF3-Containing Compounds

A simple and efficient synthesis of 2-(2,2,2-trifluoroethylidene)-1,3-dithianes is described.The title compounds are versatile intermediates for the preparation of trifluoromethyl derivatives.

Preparation of polyfluoroaldehydes and polyfluoroacetals

A group of polyfluoroaldehydes represented by 3,3,3-trifluoropropanal can be formed with very good selectivity by reacting polyfluoroalkenes represented by 3,3,3-trifluoropropene with water in the presence of a source of divalent palladium. A group of polyfluoroacetals represented by 1,1-dialkoxy-3,3,3-trifluoropropane can be formed with very good selectivity by reacting the same polyfluoroalkenes with an alcohol in the presence of a source of divalent palladium.

β-PERFLUOROALKYLVINYL ALKYL ETHERS

A convenient method was developed for the synthesis of β-perfluoroalkyl-substituted vinyl ethers by the reaction of vinyl alkyl ethers with perfluoroalkyl iodides in the presence of a palladium catalyst.Fluorine-containing aldehydes and their acetals, in which the perfluoroalkyl radical is separated from the formyl group by a methylene unit, were synthesized from the ethers.These aldehydes can be used for the synthesis of β-perfluoroalkyldicarbocyanines.