(3R,4S,5S)-3-(tert-butyldiphenylsilyloxy)-5-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-2,4-dimethylcyclopent-1-enecarbaldehyde

Base Information

• Chemical Name: (3R,4S,5S)-3-(tert-butyldiphenylsilyloxy)-5-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-2,4-dimethylcyclopent-1-enecarbaldehyde
• CAS No.: 1030607-32-9
• Molecular Formula: C₃₇H₄₆O₅Si
• Molecular Weight: 598.855

Synonyms:(3R,4S,5S)-3-(tert-butyldiphenylsilyloxy)-5-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-2,4-dimethylcyclopent-1-enecarbaldehyde

Chemical Property of (3R,4S,5S)-3-(tert-butyldiphenylsilyloxy)-5-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-2,4-dimethylcyclopent-1-enecarbaldehyde

Chemical Property:

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Technology Process of (3R,4S,5S)-3-(tert-butyldiphenylsilyloxy)-5-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-2,4-dimethylcyclopent-1-enecarbaldehyde

There total 1 articles about (3R,4S,5S)-3-(tert-butyldiphenylsilyloxy)-5-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-2,4-dimethylcyclopent-1-enecarbaldehyde 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:

C37H48O6Si → (3R,4S,5S)-3-(tert-butyldiphenylsilyloxy)-5-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-2,4-dimethylcyclopent-1-enecarbaldehyde (1030607-32-9)

Guidance literature:

With piperidine; acetic acid; In benzene; at 20 - 60 ℃; for 21h; Inert atmosphere;

DOI:10.1021/ol800419v

Reference yield:

(3R,4S,5S)-3-(tert-butyldiphenylsilyloxy)-5-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-2,4-dimethylcyclopent-1-enecarbaldehyde (1030607-32-9) → C37H46O6Si

Guidance literature:

With sodium dihydrogenphosphate; 2-methyl-but-2-ene; sodium chloride; In water; tert-butyl alcohol; at 20 ℃; for 0.5h; Inert atmosphere;

DOI:10.1021/ol800419v

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