(2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1,3-<(p-methoxybenzylidene)dioxy>-2,4,6-trimethylheptan-5-ol

Base Information

Chemical Name:(2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1,3-<(p-methoxybenzylidene)dioxy>-2,4,6-trimethylheptan-5-ol
CAS No.:124755-35-7
Molecular Formula:C₂₄H₄₂O₅Si
Molecular Weight:438.68
Hs Code.:

Synonyms:(2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1,3-<(p-methoxybenzylidene)dioxy>-2,4,6-trimethylheptan-5-ol

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Chemical Property of (2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1,3-<(p-methoxybenzylidene)dioxy>-2,4,6-trimethylheptan-5-ol

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Technology Process of (2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1,3-<(p-methoxybenzylidene)dioxy>-2,4,6-trimethylheptan-5-ol

There total 5 articles about (2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1,3-<(p-methoxybenzylidene)dioxy>-2,4,6-trimethylheptan-5-ol 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: 70.0%

: 124755-34-6
(2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1-<(p-methoxybenzyl)oxy>-2,4,6-trimethylheptane-3,5-diol

: 124755-35-7
(2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1,3-<(p-methoxybenzylidene)dioxy>-2,4,6-trimethylheptan-5-ol

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; for 2h; Ambient temperature;
DOI:10.1021/jo00292a031

Reference yield:

: 124755-27-7
(E)-(2R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-2,4,6-trimethyl-3-heptene-1,5-diol

: 124755-35-7
(2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1,3-<(p-methoxybenzylidene)dioxy>-2,4,6-trimethylheptan-5-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / tris<2-(2-methoxyethoxy)ethyl>amine, KOH / CH₂Cl₂ / 48 h / 0 °C

3: 70 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / CH₂Cl₂ / 2 h / Ambient temperature

With potassium hydroxide; Tris(3,6-dioxaheptyl)amine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane;
DOI:10.1021/jo00292a031

Reference yield:

: 124755-26-6
(Z)-(4S,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-3,5-dimethyl-3,4-epoxy-2-hepten-1-ol

: 124755-35-7
(2R,3R,4R,5R,6S)-7-<(tert-butyldimethylsilyl)oxy>-1,3-<(p-methoxybenzylidene)dioxy>-2,4,6-trimethylheptan-5-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / diethyl ether / -23 - 0 °C

2: 72 percent / tris<2-(2-methoxyethoxy)ethyl>amine, KOH / CH₂Cl₂ / 48 h / 0 °C

4: 70 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / CH₂Cl₂ / 2 h / Ambient temperature

With potassium hydroxide; Tris(3,6-dioxaheptyl)amine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In diethyl ether; dichloromethane;
DOI:10.1021/jo00292a031