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Updated: Nov 7, 2025

Synthesis of Esters Via a Greener Steglich Esterification in Acetonitrile
Published on: October 30, 2018
Interstellar Enolization-Acetaldehyde (CH3 CHO) and Vinyl Alcohol (H2 CCH(OH)) as a Case Study
N Fabian Kleimeier1, Ralf I Kaiser1
1Department of Chemistry and W. M. Keck Research Laboratory in Astrochemistry, University of Hawai'i at Manoa, 2545 McCarthy Mall, Honolulu, HI, 96822, USA.
Galactic cosmic rays (GCRs) can induce the formation of enols, less stable organic molecules, in interstellar ices. This finding suggests enols are widespread in space and can be detected by radio telescopes.
Area of Science:
- Astrochemistry
- Interstellar Medium Chemistry
- Organic Chemistry
Background:
- Enols, thermodynamically less stable tautomers, typically do not form in cold gas-phase environments.
- Laboratory studies show keto-enol pairs form in interstellar analog ices, but only acetaldehyde-vinyl alcohol has been detected in space.
- Enols' reactivity with electrophiles is key to understanding molecular complexity in the interstellar medium, comets, and meteorites.
Purpose of the Study:
- Investigate the enolization of aldehydes in interstellar ices via interaction with galactic cosmic rays (GCRs).
- Utilize energetic electrons as proxies for secondary electrons generated by GCRs in interstellar ices.
Main Methods:
- Irradiation of acetaldehyde ices with energetic electrons.
- Simulation of secondary electron interactions from GCRs in interstellar ice analogs.
Main Results:
- Galactic cosmic rays (GCRs) can induce the enolization of acetaldehyde in interstellar ices.
- Both intra- and intermolecular processes contribute to enol formation.
- Enols are likely ubiquitous in the interstellar medium.
Conclusions:
- Enols should be widespread in the interstellar medium and detectable by radio telescopes like ALMA.
- Detection of enols will enable their use as tracers for non-equilibrium ice chemistry.
- This can help constrain fundamental reaction mechanisms within interstellar ices.
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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.
Reactivity of Enols