(3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}4-methyl-pentane-1,4-diol

Base Information

Chemical Name:(3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}4-methyl-pentane-1,4-diol
CAS No.:1528746-83-9
Molecular Formula:C₂₃H₃₆O₆
Molecular Weight:408.535
Hs Code.:

Synonyms:(3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}4-methyl-pentane-1,4-diol

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Chemical Property of (3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}4-methyl-pentane-1,4-diol

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Technology Process of (3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}4-methyl-pentane-1,4-diol

There total 6 articles about (3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}4-methyl-pentane-1,4-diol 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: 100.0%

: 1528746-82-8
(3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl-4-(methoxymethoxy)-5-methylphenoxy]-5-tert-butyldiphenylsilyloxy}-2-methylpentan-2-ol

: 1528746-83-9
(3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}4-methyl-pentane-1,4-diol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 0.05h; Inert atmosphere;
DOI:10.1016/j.tet.2013.11.070

Reference yield:

: 1313708-38-1
(2R,3E)-2-[5-(benzyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenol

: 1528746-83-9
(3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}4-methyl-pentane-1,4-diol

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / acetonitrile / 4 h / 20 °C / Inert atmosphere

2.1: tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

3.1: lithium di-tert-buthylbiphenilide / tetrahydrofuran / 0.05 h / -78 °C / Inert atmosphere

4.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

4.2: 6 h / 0 - 20 °C / Inert atmosphere

5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.05 h / 20 °C / Inert atmosphere

With lithium di-tert-buthylbiphenilide; tetrabutyl ammonium fluoride; sodium hydride; potassium carbonate; In tetrahydrofuran; acetonitrile;
DOI:10.1016/j.tet.2013.11.070

Reference yield:

: 1528746-70-4
(2R)-methyl 2-{2-[(2R,3E)-5-(benzyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}-4-(tert-butyldiphenylsilyloxy)butanoate

: 1528746-83-9
(3R)-3-{2-[(2R,3E)-5-(allyloxy)pent-3-en-2-yl]-4-(methoxymethoxy)-5-methylphenoxy}4-methyl-pentane-1,4-diol

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

2.1: lithium di-tert-buthylbiphenilide / tetrahydrofuran / 0.05 h / -78 °C / Inert atmosphere

3.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

3.2: 6 h / 0 - 20 °C / Inert atmosphere

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.05 h / 20 °C / Inert atmosphere

With lithium di-tert-buthylbiphenilide; tetrabutyl ammonium fluoride; sodium hydride; In tetrahydrofuran;
DOI:10.1016/j.tet.2013.11.070