Home Chemistry Heterocyclic Building Blocks Pyrrolidines 2-Amino-1-(Pyrrolidin-1-Yl)Ethan-1-One
Nucleophilic Addition: The carbonyl group can undergo nucleophilic addition reactions with nucleophiles such as Grignard reagents, organolithium compounds, or hydride donors.
Reduction: The carbonyl group can be reduced to form the corresponding alcohols using reducing agents like lithium aluminum hydride or sodium borohydride.
Acylation: The nitrogen atom in the pyrrolidine ring can undergo acylation reactions to form N-acyl derivatives.
Substitution Reactions: The nitrogen atom can undergo substitution reactions, such as nucleophilic substitution or electrophilic substitution.
Condensation Reactions: It can participate in condensation reactions to form cyclic compounds or larger molecules.
Ring-closing Reactions: The compound may undergo intramolecular cyclization reactions to form cyclic compounds.
Oxidation: The amino group can be oxidized to form nitro compounds or other oxidation products.
Hydrolysis: Under acidic or basic conditions, amide bonds can undergo hydrolysis to regenerate the amine and carboxylic acid.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
(S)-1-(2-Aminoacetyl)-4,4-difluoropyrrolidine-2-carbonitrile hydrochloride
click to sign in and save
2-Amino-1-(pyrrolidin-1-yl)ethanone hydrochloride
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :