112700-10-4

Upstream product

• 499774-39-9 7-tert-butyl-3,3,5-trimethyl-3H-benzofuran-2-one 
• 499774-40-2 7-tert-butyl-3,3-dimethyl-2-oxo-3H-benzofuran-5-carbaldehyde 
• 112700-14-8 6-tert-butyl-2-(2'-hydroxy-1',1'-dimethylethyl)-4-methylphenol 
• 499774-41-3 7-tert-butyl-5-(1,3-dioxolan-2-yl)-3,3-dimethyl-3H-benzofuran-2-one 

Downstream Products

• 499774-44-6 2-tert-butyl-6-[1,1-dimethyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-4-[(2-ethyl-1,1-dioxo-1λ⁶-isothiazolidin-5-yl)-hydroxy-methyl]-phenol 
• 223580-82-3 (E)-5-[3-tert-butyl-4-hydroxy-5-(2-hydroxy-1,1-dimethyl-ethyl)]-benzylidene-2-ethyl-1,2-isothiazolidine-1,1-dioxide 
• 499774-43-5 3-tert-butyl-5-[1,1-dimethyl-2-(tetrahydropyran-2-yloxy)ethyl]-4-hydroxybenzaldehyde 

Relevant academic research and scientific papers

Short synthesis of tert-butyl-hydroxylated 3,5-di-tert-butyl-4-hydroxybenzaldehyde: Synthesis of tert-butyl-hydroxylated S-2474

We have developed a very short synthesis of tertbutyl-hydroxylated di-tert-butyl-4-hydroxybenzaldehyde in which the HBr-DMSO system is used as an effective oxidant (overall yield of 45% for the entire four-step process from 2-tert-butyl-p-cresol). We also accomplished the synthesis of a major metabolite of the antiarthritic drug candidate S-2474.