Doerr, Maurice published the artcileSynthesis of Highly Functionalized N,N-Diarylamides by an Anodic C,N-Coupling Reaction, Name: 4-Hydroxy-3-tert-butylanisole, the main research area is diaryl amide preparation; benzoxazole tertiary butyl methoxyphenol anodic dehydrogenative coupling; C,N-coupling; C−H activation; electrochemistry; oxidation; sustainable chemistry.
An innovative, sustainable and straightforward protocol was reported for the synthesis of N,N-diarylamides I [R1 = H, 3-Me, 4-Me, 5-Me, 3-Br, 4-Cl; R2 = H, Me, Et] equipped with nonprotected hydroxyl groups by using electrosynthesis. The concept allowed the application of various substrates furnishing diarylamides with yields up to 57 % within a single and direct electrolytic protocol. The method was thereby easy to conduct in an undivided cell with constant current conditions offering a versatile and short-cut alternative to conventional pathways.
Chemistry – A European Journal published new progress about Benzoxazoles Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 121-00-6 belongs to class ethers-buliding-blocks, name is 4-Hydroxy-3-tert-butylanisole, and the molecular formula is C11H16O2, Name: 4-Hydroxy-3-tert-butylanisole.
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem