Home Chemistry Organic Building Blocks Sulfones Tetrahydrothiophene 1,1-Dioxide
Hydrolysis: Tetrahydrothiophene 1,1-dioxide can be hydrolyzed by strong acids or bases to produce the corresponding carboxylic acid and sulfur dioxide gas.
Oxidation: Tetrahydrothiophene 1,1-dioxide can be oxidized to form various sulfur-containing compounds. For example, it can be oxidized to sulfones or sulfoxides depending on the reaction conditions and reagents.
Nucleophilic Substitution: The oxygen atom in the molecule can serve as a nucleophilic site and can undergo substitution reactions with electrophiles. For example, it can react with alkyl halides to form ethers.
Ring-Opening Reactions: Tetrahydrothiophene 1,1-dioxide can undergo ring-opening reactions under certain conditions. For instance, it can be cleaved to yield a linear compound when treated with suitable reagents.
Addition Reactions: The double bond in the thiophene ring can undergo addition reactions with electrophiles, such as halogens or electrophilic reagents, leading to the formation of addition products.
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3-(Methylamino)tetrahydrothiophene 1,1-dioxide
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(S)-3-Aminotetrahydrothiophene 1,1-dioxide hydrochloride
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3-Bromo-4-hydroxytetrahydrothiophene 1,1-dioxide
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1-(1,1-Dioxidotetrahydrothiophen-3-yl)-1,3,3-trimethylurea
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3-Aminotetrahydrothiophene 1,1-dioxide hydrochloride
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(R)-3-Aminotetrahydrothiophene 1,1-dioxide hydrochloride
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rel-(3R,4S)-3-Amino-4-chlorotetrahydrothiophene 1,1-dioxide hydrochloride
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3-Isopropoxytetrahydrothiophene 1,1-dioxide
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3-(Aminomethyl)tetrahydrothiophene 1,1-dioxide hydrochloride
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3-(Methylamino)tetrahydrothiophene 1,1-dioxide hydrochloride
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