Home Chemistry Heterocyclic Building Blocks Spiroes 2,8-Diazaspiro[4.5]Decane
Acid-Base Reactions: Like many organic amines, 2,8-diazaspiro[4.5]decane can act as a base, accepting a proton (H+) from an acid to form its conjugate acid.
Alkylation: The nitrogen atoms in the ring can be alkylated, meaning alkyl groups (-CH3, -CH2CH3, etc.) can be attached to the nitrogen atoms. This can be achieved through reactions with alkyl halides or other alkylating agents.
Acylation: Similar to alkylation, the nitrogen atoms can also undergo acylation reactions, where acyl groups (RCO-) are attached to the nitrogen atoms. This can be accomplished using acyl chlorides or anhydrides.
Redox Reactions: Depending on the specific substituents and conditions, 2,8-diazaspiro[4.5]decane can participate in redox reactions, gaining or losing electrons to form different oxidation states.
Ring-Opening Reactions: Under certain conditions, the spirocyclic ring system can undergo ring-opening reactions, breaking the ring and forming new compounds. This can be triggered by the presence of strong nucleophiles or electrophiles.
Complex Formation: Due to its unique structure, 2,8-diazaspiro[4.5]decane can form complexes with various metal ions. These complexes can have interesting properties and may be used in coordination chemistry.
Substitution Reactions: Substitution reactions at various positions within the molecule are possible, depending on the reagents and conditions used.
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tert-Butyl 2,8-diazaspiro[4.5]decane-8-carboxylate HCl
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tert-butyl 2,8-diazaspiro[4.5]decane-8-carboxylate
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8-Methyl-2,8-diazaspiro[4.5]decane dihydrochloride
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tert-butyl 2,8-diazaspiro[4.5]decane-2-carboxylate
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2,8-Diazaspiro[4.5]decane dihydrochloride
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