Home Chemistry Heterocyclic Building Blocks Pyrrolidines 2-(Methoxymethyl)Pyrrolidine
Nucleophilic Substitution: The methoxy group can undergo nucleophilic substitution reactions, such as displacement by a nucleophile, resulting in the formation of different substituted pyrrolidine derivatives.
Ring-opening Reactions: The pyrrolidine ring may undergo ring-opening reactions under certain conditions, leading to the formation of linear or branched compounds.
Alkylation: The nitrogen atom in the pyrrolidine ring can be alkylated by reaction with alkyl halides or sulfonates.
Oxidation: The methoxy group can undergo oxidation reactions under specific conditions, leading to the formation of various oxidation products.
Reduction: The carbonyl group in the methoxymethyl moiety can be reduced to a hydroxyl group or an alkyl group.
Etherification: The methoxy group can undergo etherification reactions with alcohol or alkoxide reagents, forming ether derivatives.
Hydrolysis: Under acidic or basic conditions, the ether linkage can undergo hydrolysis to regenerate the alcohol and pyrrolidine.
Condensation Reactions: It can participate in condensation reactions with carbonyl compounds or other nucleophiles to form cyclic compounds or larger molecules.
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(R)-tert-Butyl 2-(methoxymethyl)pyrrolidine-1-carboxylate
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(S)-(-)-1-Amino-2-(methoxymethyl)pyrrolidine
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(R)-2-(Methoxymethyl)pyrrolidine hydrochloride
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2-(Methoxymethyl)pyrrolidine-1-sulfonyl chloride
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