(2R,3S,4R)-2-(4-methoxybenzyloxy)-4-methylhex-5-en-3-yl (2R,3S,4S,6R)-3,7-bis(tert-butyldimethylsilyloxy)-2,4,6-trimethylheptanoate

Base Information

Chemical Name:(2R,3S,4R)-2-(4-methoxybenzyloxy)-4-methylhex-5-en-3-yl (2R,3S,4S,6R)-3,7-bis(tert-butyldimethylsilyloxy)-2,4,6-trimethylheptanoate
CAS No.:1234550-50-5
Molecular Formula:C₃₇H₆₈O₆Si₂
Molecular Weight:665.114
Hs Code.:

Synonyms:(2R,3S,4R)-2-(4-methoxybenzyloxy)-4-methylhex-5-en-3-yl (2R,3S,4S,6R)-3,7-bis(tert-butyldimethylsilyloxy)-2,4,6-trimethylheptanoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2R,3S,4R)-2-(4-methoxybenzyloxy)-4-methylhex-5-en-3-yl (2R,3S,4S,6R)-3,7-bis(tert-butyldimethylsilyloxy)-2,4,6-trimethylheptanoate

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Technology Process of (2R,3S,4R)-2-(4-methoxybenzyloxy)-4-methylhex-5-en-3-yl (2R,3S,4S,6R)-3,7-bis(tert-butyldimethylsilyloxy)-2,4,6-trimethylheptanoate

There total 1 articles about (2R,3S,4R)-2-(4-methoxybenzyloxy)-4-methylhex-5-en-3-yl (2R,3S,4S,6R)-3,7-bis(tert-butyldimethylsilyloxy)-2,4,6-trimethylheptanoate 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: 97.0%

: 1234550-38-9
(2R,3S,4R)-2-(4-methoxybenzyloxy)-4-methylhex-5-en-3-ol

: 1234550-49-2
C₂₂H₄₈O₄Si₂

: 1234550-50-5
(2R,3S,4R)-2-(4-methoxybenzyloxy)-4-methylhex-5-en-3-yl (2R,3S,4S,6R)-3,7-bis(tert-butyldimethylsilyloxy)-2,4,6-trimethylheptanoate

Guidance literature:: C₂₂H₄₈O₄Si₂; With 2,4,6-trichlorobenzoyl chloride; triethylamine; In tetrahydrofuran; at 20 ℃; for 3h;

(2R,3S,4R)-2-(4-methoxybenzyloxy)-4-methylhex-5-en-3-ol; With dmap; In benzene; for 15h;
DOI:10.1016/j.tet.2010.04.039