182250-68-6

Usage

Uses

Used in Organic Synthesis:
3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZOIC ACID METHYL ESTER is used as a reagent for the protection and deprotection of hydroxyl groups in organic molecules, facilitating the synthesis of complex organic compounds.
Used in Pharmaceutical Industry:
3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZOIC ACID METHYL ESTER is used as a building block in the synthesis of various biologically active compounds and pharmaceuticals, contributing to the development of new drugs and therapies.
Used in Research:
3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZOIC ACID METHYL ESTER is used as a versatile chemical in the field of organic chemistry research, enabling the exploration of new reactions and the creation of novel organic molecules.

InChI:InChI=1/C40H44O4Si2/c1-39(2,3)45(34-20-12-8-13-21-34,35-22-14-9-15-23-35)43-32-28-31(38(41)42-7)29-33(30-32)44-46(40(4,5)6,36-24-16-10-17-25-36)37-26-18-11-19-27-37/h8-30H,1-7H3

Upstream product

• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 99-10-5 3,5-Dihydroxybenzoic acid 

Downstream Products

• 182250-70-0 3,5-di-(tert-butyl(diphenyl)silyloxy)benzyl alcohol 
• 150551-00-1 3,5-bis(3,5-bis(4-methoxycarbonylphenyl)benzyloxy)benzyl alcohol 

Relevant academic research and scientific papers

Synthesis of Benzo[ b]furans by Intramolecular C-O Bond Formation Using Iron and Copper Catalysis

One-pot processes for the synthesis of benzo[b]furans from 1-aryl- or 1-alkylketones using nonprecious transition metal catalysts have been developed. Regioselective iron(III)-catalyzed halogenation of the aryl ring, followed by iron- or copper-catalyzed O-arylation allowed the synthesis of various structural analogues, including the benzo[b]furan-derived natural products corsifuran C, moracin F, and caleprunin B.

A simple method for controlling dendritic architecture and diversity: A parallel monomer combination approach

A novel parallel monomer combination approach to manipulating the architectural disposition of dendritic macromolecules is described. It harnesses the synthetic speed and power of the double-stage convergent growth approach and classical parallel synthesi

Alternative convergent and accelerated double-stage convergent approaches towards functionalized dendritic polyethers

Alternative convergent synthesis strategies for the preparation of dendritic macromolecules, using either mesylate activation or the Mitsunobu reaction, are described. The synthesis can be further accelerated by using a double stage convergent approach. T

A fast double-stage convergent synthesis of dendritic polyethers

Two tert-butyldiphenylsilyl-protected synthons 7 and 9 are prepared in excellent yields and used in a one-pot synthesis of higher generation polyether dendrons.