Home Chemistry Heterocyclic Building Blocks Spiroes 1,4-Dioxaspiro[4.5]Decane
Hydrolysis: 1,4-dioxaspiro[4.5]decane can undergo hydrolysis under acidic or basic conditions, leading to the cleavage of the spiro ring system and the formation of diols or other products.
Oxidation: The compound can be oxidized using various oxidizing agents to produce different oxidation products, depending on the reaction conditions.
Grignard Reaction: It can react with Grignard reagents to form new carbon-carbon bonds and functionalize the molecule.
Reduction: The compound can be reduced to form saturated derivatives using reducing agents such as sodium borohydride or lithium aluminum hydride.
Halogenation: It can undergo halogenation reactions (e.g., chlorination or bromination) to introduce halogen atoms into the molecule.
Nucleophilic Substitution: Under suitable conditions, it can participate in nucleophilic substitution reactions, depending on the nucleophile and reaction conditions.
Ring-opening reactions: The spiro ring system can be cleaved under various conditions to open the structure and generate new compounds.
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(6-Isopropyl-9-methyl-1,4-dioxaspiro[4.5]decan-2-yl)methanol
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Ethyl 1,4-dioxaspiro[4.5]decane-8-carboxylate
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1,4-Dioxaspiro[4.5]decane-8-carboxylic acid
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8-Amino-1,4-dioxaspiro[4.5]decane-8-carboxylic Acid
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Ethyl 8-methyl-1,4-dioxaspiro[4.5]decane-8-carboxylate
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Methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate
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