(2R,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-enal

Base Information

• Chemical Name: (2R,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-enal
• CAS No.: 1030594-87-6
• Molecular Formula: C₂₆H₄₄O₄Si
• Molecular Weight: 448.718

Synonyms:(2R,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-enal

Chemical Property of (2R,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-enal

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Technology Process of (2R,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-enal

There total 1 articles about (2R,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-enal 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%

(2S,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-en-1-ol (1030594-85-4) → (2R,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-enal (1030594-87-6)

Guidance literature:

With 2,2,6,6-tetramethyl-piperidine-N-oxyl; [bis(acetoxy)iodo]benzene; In dichloromethane; at 20 ℃;

DOI:10.1016/j.tetlet.2008.02.099

Reference yield: 83.0%

(2R,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-enal (1030594-87-6) + (S)-3-propanoyl-4-benzyl-1,3-thiazolidine-2-thione (263764-23-4,863324-53-2) → (2R,3S,4S,5S,6S,8R,9R)-1-[(S)-4-benzyl-2-thioxothiazolidin-3-yl]-9-(tert-butyldimethylsilyloxy)-3-hydroxy-5-(4-methoxybenzyloxy)-2,4,6,8-tetramethylundec-10-en-1-one (1030594-89-8)

Guidance literature:

With titanium tetrachloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃;

DOI:10.1016/j.tetlet.2008.02.099

upstream raw materials:

(2S,3S,4S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3-(4-methoxybenzyloxy)-2,4,6-trimethylnon-8-en-1-ol

Downstream raw materials:

(2R,3S,4S,5S,6S,8R,9R)-1-[(S)-4-benzyl-2-thioxothiazolidin-3-yl]-9-(tert-butyldimethylsilyloxy)-3-hydroxy-5-(4-methoxybenzyloxy)-2,4,6,8-tetramethylundec-10-en-1-one

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