(+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-2-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)propane

Base Information

Chemical Name:(+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-2-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)propane
CAS No.:745809-53-4
Molecular Formula:C₃₀H₅₀O₄Si₂
Molecular Weight:530.896
Hs Code.:

Synonyms:(+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-2-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)propane

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Chemical Property of (+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-2-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)propane

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Technology Process of (+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-2-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)propane

There total 4 articles about (+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-2-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)propane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 745809-30-7
(+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-3-(4-methoxybenzyloxy)propan-2-ol

: 745809-53-4
(+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-2-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)propane

Guidance literature:: With 1H-imidazole; dmap; In dichloromethane; at 0 - 23 ℃;
DOI:10.1021/jo049426c

Reference yield:

: 34946-83-3
2,4,4,6-tetrabromo-3-methyl-cyclohexa-2,5-dienone

: 745809-53-4
(+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-2-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)propane

Guidance literature:: Multi-step reaction with 3 steps

1: 57 percent / sulfuric acid / 16 h

2: 2,6-lutidine

With 2,6-dimethylpyridine; sulfuric acid;
DOI:10.1021/jo049426c

Reference yield:

: 108-39-4
3-methyl-phenol

: 745809-53-4
(+)-1-[3-(tert-butyldimethylsilyloxy)-5-methylphenyl]-2-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)propane

Guidance literature:: Multi-step reaction with 4 steps

1: 52 percent / Br₂ / acetic acid

2: 57 percent / sulfuric acid / 16 h

3: 2,6-lutidine

With 2,6-dimethylpyridine; sulfuric acid; bromine; In acetic acid;
DOI:10.1021/jo049426c