(2R,3R,4S,5R,6R)-5-[(4-methoxybenzyl)oxy]-2,4,6-trimethylheptane-1,3,7-triol

Base Information

Chemical Name:(2R,3R,4S,5R,6R)-5-[(4-methoxybenzyl)oxy]-2,4,6-trimethylheptane-1,3,7-triol
CAS No.:1158302-56-7
Molecular Formula:C₁₈H₃₀O₅
Molecular Weight:326.433
Hs Code.:

Synonyms:(2R,3R,4S,5R,6R)-5-[(4-methoxybenzyl)oxy]-2,4,6-trimethylheptane-1,3,7-triol

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Chemical Property of (2R,3R,4S,5R,6R)-5-[(4-methoxybenzyl)oxy]-2,4,6-trimethylheptane-1,3,7-triol

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Technology Process of (2R,3R,4S,5R,6R)-5-[(4-methoxybenzyl)oxy]-2,4,6-trimethylheptane-1,3,7-triol

There total 1 articles about (2R,3R,4S,5R,6R)-5-[(4-methoxybenzyl)oxy]-2,4,6-trimethylheptane-1,3,7-triol 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: 90.0%

: C₁₈H₂₄O₅

: 1158302-56-7
(2R,3R,4S,5R,6R)-5-[(4-methoxybenzyl)oxy]-2,4,6-trimethylheptane-1,3,7-triol

Guidance literature:: C₁₈H₂₄O₅; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 25 ℃;

With water; ammonium chloride; In tetrahydrofuran; at 0 ℃;
DOI:10.1016/j.tet.2008.12.049

Reference yield: 92.0%

: 1158302-56-7
(2R,3R,4S,5R,6R)-5-[(4-methoxybenzyl)oxy]-2,4,6-trimethylheptane-1,3,7-triol

: 77-76-9
2,2-dimethoxy-propane

: 1158302-78-3
(2R,3R,4R)-3-(4-methoxybenzyloxy)-2-methyl-4-[2,2,5-trimethyl-(4S,5S)-1,3-dioxan-4-yl]pentan-1-ol

Guidance literature:: With camphor-10-sulfonic acid; In diethyl ether; dichloromethane; at 20 ℃; for 1h;
DOI:10.1016/j.tet.2008.12.049

Reference yield:

: 1158302-56-7
(2R,3R,4S,5R,6R)-5-[(4-methoxybenzyl)oxy]-2,4,6-trimethylheptane-1,3,7-triol

: C₄₀H₆₂O₅Si₂

Guidance literature:: Multi-step reaction with 4 steps

1: camphor-10-sulfonic acid / dichloromethane / 1 h / 0 - 20 °C

2: 1H-imidazole / dichloromethane / 2 h / 0 - 20 °C

3: copper(II) choride dihydrate / acetonitrile / 0.5 h / 0 °C

4: 1H-imidazole / dichloromethane / 2 h / 0 - 20 °C

With 1H-imidazole; copper(II) choride dihydrate; camphor-10-sulfonic acid; In dichloromethane; acetonitrile;
DOI:10.1016/j.tetlet.2018.06.020