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Applications of 5-tert-butyl-2-iodophenol ( CAS No. 20942-70-5)

https://www.pudeepharm.com/news/20942-70-5-2/5-tert-Butyl-2-iodophenol (CAS No. 20942-70-5) is an iodinated phenolic derivative characterized by a bulky tert-butyl substituent at the meta-position (relative to the hydroxyl group) and an iodine atom at the ortho-position. This specific substitution pattern makes it a valuable building block in organic synthesis, particularly for the construction of complex heterocyclic frameworks and sterically hindered molecules.

  1. Physical and Chemical Properties

The compound typically appears as colorless to white crystalline needles or a pale yellow solid. Its chemical behavior is dictated by the reactivity of the phenol group, the steric bulk of the tert-butyl group, and the labile nature of the carbon-iodine (C-I) bond.

  • Molecular Formula: C10H13IO
  • Melting Point: 49--51°C
  • Solubility: Soluble in common organic solvents such as benzene, chloroform, hexane, and methanol; poorly soluble in water.
  • Reactivity: The presence of the iodine atom at the ortho-position (position 2) allows for diverse transition metal-catalyzed coupling reactions. The tert-butyl group at position 5 provides steric protection and enhances the lipophilicity of the molecule.
  1. Industrial and Synthetic Applications

While 5-tert-butyl-2-iodophenol is primarily utilized as a research chemical and specialty intermediate, its industrial relevance lies in the production of high-value fine chemicals.

Synthesis of Benzofuran Derivatives

The compound serves as a critical starting material for the synthesis of 2-substituted benzofurans, which are essential building blocks in the pharmaceutical industry for developing anti-inflammatory and anti-fungal agents. It can undergo nickel-catalyzed or palladium-catalyzed intermolecular cyclization with terminal alkynes to form these bicyclic structures.

Cross-Coupling and Biaryl Synthesis

The C-I bond is highly reactive in Suzuki-Miyaura and Sonogashira coupling reactions. It is used to synthesize substituted biaryls and nitro-biaryl-ols, which are precursors for advanced heterocycles like carbazoles.

Polymer and Additive Chemistry

Iodinated phenols are often explored as intermediates for high-refractive-index polymers or as flame retardants. The tert-butyl group specifically improves the thermal stability and antioxidant properties of the resulting derivatives.

Product:20942-70-5