Home Chemistry Heterocyclic Building Blocks Piperidines Tert-Butyl (Piperidin-3-Ylmethyl)Carbamate
Hydrolysis: The carbamate group can undergo hydrolysis under acidic or basic conditions to yield tert-butylamine and piperidin-3-ol.
Substitution Reactions: The carbamate group can undergo nucleophilic substitution reactions with various electrophiles, leading to the formation of substituted carbamates.
Alkylation: The nitrogen atom in the piperidine ring can be alkylated by reaction with alkyl halides or sulfonates.
Reduction: The carbonyl group of the carbamate can be reduced to the corresponding alcohols using reducing agents such as lithium aluminum hydride or sodium borohydride.
Acylation: The nitrogen atom in the piperidine ring can undergo acylation reactions to form N-acyl derivatives.
Ring-opening Reactions: The piperidine ring may undergo ring-opening reactions under certain conditions, leading to the formation of linear or branched compounds.
Condensation Reactions: It can participate in condensation reactions with carbonyl compounds or other nucleophiles to form cyclic compounds or larger molecules.
Protonation: The amine group can be protonated under acidic conditions to form the corresponding ammonium salt.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
(R)-tert-Butyl (piperidin-3-ylmethyl)carbamate hydrochloride
click to sign in and save
(R)-tert-Butyl (piperidin-3-ylmethyl)carbamate
click to sign in and save
(S)-tert-butyl (piperidin-3-ylmethyl)carbamate
click to sign in and save
tert-Butyl (piperidin-3-ylmethyl)carbamate hydrochloride
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :