Home Chemistry Heterocyclic Building Blocks Piperidines Tert-Butyl 3-Bromopiperidine-1-Carboxylate
Nucleophilic Substitution: The bromine atom can undergo nucleophilic substitution reactions with various nucleophiles, leading to the formation of substituted piperidine derivatives.
Reduction: The carbonyl group of the ester moiety can be reduced to the corresponding alcohols using reducing agents such as lithium aluminum hydride or sodium borohydride.
Ring-opening Reactions: The piperidine ring may undergo ring-opening reactions under certain conditions, leading to the formation of linear or branched compounds.
Acylation: The nitrogen atom in the piperidine ring can undergo acylation reactions to form N-acyl derivatives.
Substitution Reactions: The ester group can undergo substitution reactions, such as nucleophilic substitution or electrophilic substitution.
Hydrolysis: The ester group can undergo hydrolysis under acidic or basic conditions to form the corresponding carboxylic acids and alcohols.
Decarboxylation: Under certain conditions, such as heating or treatment with specific reagents, decarboxylation may occur, leading to the loss of the carboxyl group and formation of the corresponding amine.
Condensation Reactions: It can participate in condensation reactions with carbonyl compounds or other nucleophiles to form cyclic compounds or larger molecules.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
(S)-tert-Butyl 3-bromopiperidine-1-carboxylate
click to sign in and save
tert-Butyl 3-bromo-4,4-difluoropiperidine-1-carboxylate
click to sign in and save
(R)-tert-Butyl 3-bromopiperidine-1-carboxylate
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :