Home Chemistry Heterocyclic Building Blocks Thiophenes Dibenzo[B,D]Thiophene
Electrophilic Aromatic Substitution: Dibenzo[b,d]thiophene can undergo typical electrophilic aromatic substitution reactions, where electrophiles react with the electron-rich aromatic ring to substitute hydrogen atoms. Common electrophiles include halogens (chlorination, bromination, iodination), nitration, sulfonation, and Friedel-Crafts acylation or alkylation.
Oxidation: Dibenzo[b,d]thiophene can be oxidized to produce various compounds, such as dibenzo[b,d]thiophene S-oxide or dibenzo[b,d]thiophene dioxide.
Reduction: Reduction reactions can reduce the sulfur atom in the thiophene ring. For example, hydrogenation can convert the sulfur into a saturated ring or reduce other functional groups.
Cross-Coupling Reactions: Dibenzo[b,d]thiophene can be used as a substrate in cross-coupling reactions, such as Suzuki coupling or Heck coupling, to form C-C bonds with other organic compounds.
Halogenation of Side Chains: The side chains of dibenzo[b,d]thiophene can be halogenated using various halogenation reagents.
Nucleophilic Substitution: The compound can undergo nucleophilic substitution reactions if suitable electrophilic sites are present on the molecule. For instance, nucleophiles can displace certain functional groups or atoms in the compound.
Functional Group Transformations: Chemical reactions can be used to modify or add functional groups to dibenzo[b,d]thiophene, such as esterification, amidation, or other group transformations.
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3,7-Bis(methylthio)dibenzo[b,d]thiophene
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