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Triethyl orthoacetate
[CAS# 78-39-7]

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Complete supplier list of Triethyl orthoacetate
Identification
Classification Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyrimidine compound >> Chloropyrimidine
Name Triethyl orthoacetate
Molecular Structure CAS # 78-39-7, Triethyl orthoacetate
Molecular Formula C8H18O3
Molecular Weight 162.23
CAS Registry Number 78-39-7
EC Number 201-112-4
SMILES CCOC(C)(OCC)OCC
Properties
Density 0.885
Boiling point 142 ºC
Refractive index 1.395-1.398
Flash point 36 ºC
Water solubility SLIGHTLY SOLUBLE
Safety Data
Hazard Symbols symbol symbol   GHS02;GHS07 Warning    Details
Hazard Statements H226-H315-H319-H335    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P261-P264-P264+P265-P271-P280-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P370+P378-P403+P233-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Flammable liquidsFlam. Liq.3H226
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2AH319
Transport Information UN 3272
SDS Available
up Discovory and Applicatios
Triethyl orthoacetate, a versatile chemical reagent, was first synthesized in the early 20th century as organic chemists explored the reactivity of ortho esters. This compound is characterized by its tri-ethoxy substitution pattern on an acetate moiety, giving it the formula C8H16O3. The systematic exploration of such compounds was driven by the quest for new reagents that could facilitate a variety of synthetic transformations in organic chemistry. The synthesis of triethyl orthoacetate was a significant milestone, providing researchers with a novel tool for the construction of complex organic molecules.

One of the primary uses of triethyl orthoacetate is in the formation of acetals. Acetals are important protective groups for carbonyl compounds in organic synthesis. Triethyl orthoacetate reacts with aldehydes or ketones to form stable acetals, protecting the carbonyl group from further reactions. This application is crucial in multi-step synthetic processes where selective protection and deprotection of functional groups are necessary.

Triethyl orthoacetate is employed in the synthesis of various heterocyclic compounds. Heterocycles, which contain atoms such as nitrogen, oxygen, or sulfur within a ring structure, are fundamental components of many pharmaceuticals and natural products. Triethyl orthoacetate can participate in cyclization reactions, facilitating the construction of these biologically important structures.

In nucleophilic substitution reactions, triethyl orthoacetate serves as an ethylating agent. It can transfer ethyl groups to nucleophiles, enabling the formation of ethylated products. This property is valuable in modifying the structure and properties of organic molecules, leading to the synthesis of new compounds with potential applications in materials science and pharmaceuticals.

Beyond specific reactions, triethyl orthoacetate is also used as a solvent and reagent in various organic synthesis protocols. Its unique reactivity and solvent properties can enhance the efficiency and selectivity of chemical transformations, making it a versatile tool in the chemist's arsenal.

In the pharmaceutical industry, triethyl orthoacetate is used as an intermediate in the synthesis of active pharmaceutical ingredients (APIs). Its role in constructing complex organic frameworks is crucial for the development of new drugs and therapies. By enabling the efficient synthesis of key intermediates, it contributes to the overall process of drug discovery and development.
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