Related Experiment Video
Updated: Feb 23, 2026

Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
SET-LRP in the Neoteric Ethyl Lactate Alcohol
Adrian Moreno1, Diego Garcia1, Marina Galià1
1Laboratory of Sustainable Polymers, Department of Analytical Chemistry and Organic Chemistry, University Rovira i Virgili , Tarragona, Spain.
Ethyl lactate (EtLa) is a green solvent suitable for Atom Transfer Radical Polymerization (ATRP) techniques like SET-LRP. It enables the synthesis of functional polyacrylates, expanding green chemistry applications in biomaterials.
Area of Science:
- Polymer Chemistry
- Green Chemistry
Background:
- Ethyl lactate (EtLa) is a biodegradable and eco-friendly solvent derived from biological sources.
- Its properties, including dissolving various monomers and mediating copper-catalyzed reactions, make it a potential candidate for controlled polymerization techniques.
Purpose of the Study:
- To evaluate ethyl lactate as a green solvent for Surface-Initiated Atom Transfer Radical Polymerization (SET-LRP).
- To synthesize hydrophilic and hydrophobic polyacrylates with controlled chain-end functionality using EtLa as a solvent.
Main Methods:
- Utilized Cu(0) wire catalysis for SET-LRP.
- Employed ethyl lactate as the solvent system.
- Synthesized polyacrylates with precise chain-end functionality.
Main Results:
- Ethyl lactate effectively dissolved necessary reagents and monomers.
- The SET-LRP process in EtLa yielded both hydrophilic and hydrophobic polyacrylates.
- Achieved precise control over polymer chain end functionality.
Conclusions:
- Ethyl lactate is an excellent green solvent for SET-LRP, enabling the synthesis of functional polyacrylates.
- This expands the range of environmentally friendly solvents for ATRP techniques.
- The findings support the use of EtLa in biomacromolecule and bioconjugate synthesis for biomedical applications.
More Related Videos
10:18Extraction of Lignin with High β-O-4 Content by Mild Ethanol Extraction and Its Effect on the Depolymerization Yield
Published on: January 7, 2019
06:45Author Spotlight: Optimizing Hollow-Fiber Membranes for Continuous Liquid-Liquid Extraction of Medium-Chain Fatty Acids
Published on: August 9, 2024
Related Concept Videos
Crossed Aldol Reaction Using Strong Bases: Directed Aldol Reaction
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Preparation of Alcohols via Substitution Reactions
Alcohols can be synthesized from alkyl halides via nucleophilic substitution reactions. The highly polar carbon-halogen bond in the substrate makes halide a good leaving group. The hydroxide ion or water can act as a nucleophile to take the place of halide and form an alcohol. The substitution reactions occur via two different reaction pathways, SN1 or SN2, depending on the nature of carbon attached to the halide.
Primary alcohols are synthesized from primary alkyl halides, and the...
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration
Ethers can also be prepared from alkenes through acid-catalyzed addition of alcohols and alkoxymercuration–demercuration.
Preparation of Ethers by Acid-Catalyzed Addition of Alcohol to Alkenes
The acid-catalyzed addition of alcohol to an alkene involves treating the alkene with an excess of alcohol in the presence of an acid catalyst to form an ether under suitable conditions. The hydrogen will add to the less substituted carbon so that the nucleophile can attack the more substituted...