Home Chemistry Heterocyclic Building Blocks Oxazolidines 4-Isopropyloxazolidine
Ring-opening reactions: Oxazolidine rings can be cleaved open to form amine and alcohol groups. This can be achieved through acid-catalyzed hydrolysis or other ring-opening reactions.
Nucleophilic substitution: The nitrogen atom in the oxazolidine ring can act as a nucleophile, and the compound can undergo substitution reactions with electrophiles. For example, it can react with alkyl halides to form new substituted oxazolidine derivatives.
Reductive reactions: 4-Isopropyloxazolidine may undergo reductive reactions with reducing agents such as lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to convert functional groups within the molecule.
Oxidation reactions: Oxazolidine compounds can undergo oxidation reactions, converting the nitrogen atom to an oxo group (N-oxide) under specific conditions.
Grignard reactions: If there are suitable functional groups, the compound may react with Grignard reagents to form new carbon-carbon bonds.
Acid-catalyzed reactions: 4-Isopropyloxazolidine can undergo acid-catalyzed reactions, including hydrolysis, acetal formation, or other transformations depending on the reaction conditions and the functional groups present.
Reduction of the oxazolidine ring: The oxazolidine ring may be reduced to a saturated aminomethyl group under certain reaction conditions.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
(S)-4-Isopropyl-3-(5,5,5-trifluoropentanoyl)oxazolidin-2-one
click to sign in and save
(R)-4-Isopropyl-3-propionyloxazolidin-2-one
click to sign in and save
(S)-4-Isopropyl-3-propionyloxazolidin-2-one
click to sign in and save
(S)-4-Isopropyl-5,5-dimethyloxazolidin-2-one
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :