Home Chemistry Heterocyclic Building Blocks Pyrans Tetrahydro-2H-Pyran-2-One
Hydrolysis: GBL can be hydrolyzed under basic or acidic conditions to form gamma-hydroxybutyric acid (GHB). This is a well-known reaction and is of interest due to the use of GHB as a recreational drug.
Reduction: GBL can be reduced to form gamma-butyric acid. This reduction can be achieved using a variety of reducing agents, such as lithium aluminum hydride (LiAlH4).
Esterification: GBL can be esterified to form various gamma-butyrolactone derivatives. This reaction is typically carried out using acyl chlorides or anhydrides in the presence of a suitable base or acid catalyst.
Cyclization: GBL can undergo intramolecular cyclization reactions under certain conditions to form cyclic compounds. This depends on the reaction conditions and reagents used.
Oxidation: GBL can be oxidized to yield various compounds, depending on the oxidizing agent and conditions. This can lead to the formation of different functional groups.
Alkylation: GBL can undergo alkylation reactions, where alkyl groups are introduced onto the lactone ring. This reaction can be achieved using alkyl halides and a suitable base.
Dehydration: GBL can be dehydrated to form crotonolactone. This reaction typically involves the removal of water from the lactone ring.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
click to sign in and save
2,3,4,6-Tetra-O-trimethylsilyl-D-glucono-1,5-lactone
click to sign in and save
(S)-tert-Butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :