169376-35-6

Usage

Uses

Used in Perfume Industry:
ETHYL-2-PYRROLOYL-ACETATE is used as a flavoring and fragrance ingredient for its sweet, fruity scent with floral and woody notes, enhancing the aroma profiles of perfumes and creating a pleasant olfactory experience.
Used in Food Industry:
In the food industry, ETHYL-2-PYRROLOYL-ACETATE is utilized as a component in artificial fruit flavors, adding a natural and appealing taste to various food products.
Used in Cosmetics Industry:
ETHYL-2-PYRROLOYL-ACETATE is employed in the formulation of scented products such as soaps and lotions, where it imparts a pleasant fragrance and contributes to the overall sensory appeal of these products.
Used in Pharmaceutical Manufacturing:
ETHYL-2-PYRROLOYL-ACETATE also serves as a solvent and is involved in the manufacturing process of pharmaceuticals, playing a role in the development of various medicinal compounds.
Used in Chemical Compounds Production:
ETHYL-2-PYRROLOYL-ACETATE is used in the production of other chemical compounds, highlighting its versatility and importance in the realm of chemical synthesis.

Upstream product

• 36239-09-5 ethyl chlorocarbonylacetate 
• 1072-83-9 2-Acetylpyrrole 
• 105-58-8 Diethyl carbonate 

Relevant academic research and scientific papers

Bromide-Mediated C-H Bond Functionalization: Intermolecular Annulation of Phenylethanone Derivatives with Alkynes for the Synthesis of 1-Naphthols

Bromide-mediated intermolecular annulation of phenylethanone derivatives with alkynes has been developed, which allows for the regioselective formation of polysubstituted 1-naphthols. The usage of readily available bromine catalyst, broad substrate scope, and mild conditions make this protocol very practical. Mechanistic investigations reveal that the bromination of phenylethanone derivatives occurs to yield bromo-substituted intermediates, which react in situ with alkynes to furnish the desired 1-naphthols.

1,5-Diketones Synthesis via Three-Component Cascade Reaction

A mild and efficient cascade synthesis of 1,5-diketones from readily available N,N-dicyclohexylmethylamine, 1,3-dicarbonyl compounds, and trifluoromethyl β-diketones has been developed. This cascade reaction occurs via an oxidation/Mannich reaction/Cope elimination/Michael addition/retro-Claisen reaction sequence, and provides multiple C-C bond formations in one pot. In addition, exquisite chemoselectivity is achieved in the reaction between 1,3-dicarbonyl compounds and trifluoromethyl β-diketones.