Home Chemistry Heterocyclic Building Blocks Spiroes 3-Phenyloxetane
Ring Opening: 3-Phenyloxetane can undergo ring-opening reactions when subjected to appropriate reagents or conditions. For example, it can be opened using acids or bases, leading to the formation of an alcohol or phenol and an aldehyde or ketone, depending on the reaction conditions.
Nucleophilic Substitution: 3-Phenyloxetane can react with nucleophiles, such as amines or alkoxides, to replace the oxygen atom with the nucleophile, resulting in the formation of substituted oxetane derivatives.
Oxidation: Oxetanes can undergo oxidation reactions when exposed to oxidizing agents. This can lead to the formation of various products, such as ketones or acids, depending on the reaction conditions.
Reduction: 3-Phenyloxetane can be reduced to produce a substituted tetrahydrofuran derivative. This can be achieved using reducing agents like sodium borohydride (NaBH4).
Grignard Reaction: Grignard reagents can be used to react with 3-Phenyloxetane, leading to the formation of complex organic compounds.
Esterification: 3-Phenyloxetane can undergo esterification reactions, where it reacts with carboxylic acids or acid chlorides to form oxetane derivatives with ester functional groups.
Rearrangements: In some cases, rearrangement reactions can occur with oxetanes, leading to the formation of different products.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
tert-Butyl (3-(4-bromophenyl)oxetan-3-yl)carbamate
click to sign in and save
3-(4-Chlorophenyl)oxetan-3-amine hydrochloride
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :