(2R,3R,4S)-3-(benzyloxy)-4-((R)-2,2-dimethyl-1,3-dioxan-4-yl)-2-methylpentan-1-ol

Base Information

Chemical Name:(2R,3R,4S)-3-(benzyloxy)-4-((R)-2,2-dimethyl-1,3-dioxan-4-yl)-2-methylpentan-1-ol
CAS No.:477781-63-8
Molecular Formula:C₁₉H₃₀O₄
Molecular Weight:322.445
Hs Code.:

Synonyms:(2R,3R,4S)-3-(benzyloxy)-4-((R)-2,2-dimethyl-1,3-dioxan-4-yl)-2-methylpentan-1-ol

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Chemical Property of (2R,3R,4S)-3-(benzyloxy)-4-((R)-2,2-dimethyl-1,3-dioxan-4-yl)-2-methylpentan-1-ol

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Technology Process of (2R,3R,4S)-3-(benzyloxy)-4-((R)-2,2-dimethyl-1,3-dioxan-4-yl)-2-methylpentan-1-ol

There total 5 articles about (2R,3R,4S)-3-(benzyloxy)-4-((R)-2,2-dimethyl-1,3-dioxan-4-yl)-2-methylpentan-1-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: 95.0%

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

: 477781-62-7
(3R,4S,5R,6R)-5-(benzyloxy)-4,6-dimethylheptane-1,3,7-triol

: 477781-63-8
(2R,3R,4S)-3-(benzyloxy)-4-((R)-2,2-dimethyl-1,3-dioxan-4-yl)-2-methylpentan-1-ol

Guidance literature:: With camphor-10-sulfonic acid; In dichloromethane; at 25 ℃; for 1h;
DOI:10.1016/S0040-4039(02)01705-7

Reference yield:

: 238757-51-2
(1S,5R,6S,7S,8S)-7-Benzyloxy-6,8-dimethyl-2,9-dioxa-bicyclo[3.3.1]nonan-3-one

: 477781-63-8
(2R,3R,4S)-3-(benzyloxy)-4-((R)-2,2-dimethyl-1,3-dioxan-4-yl)-2-methylpentan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / LAH / tetrahydrofuran / 4 h / 0 - 20 °C

2: 73 percent / CSA / acetone / 3 h

With lithium aluminium tetrahydride; camphor-10-sulfonic acid; In tetrahydrofuran; acetone;
DOI:10.1016/j.tetlet.2004.06.121

Reference yield:

: 96691-92-8
(1R,2R,3r,4S,5S)-3-(benzyloxy)-2,4-dimethyl-8-oxa-bicyclo[3.2.1]oct-6-ene

: 477781-63-8
(2R,3R,4S)-3-(benzyloxy)-4-((R)-2,2-dimethyl-1,3-dioxan-4-yl)-2-methylpentan-1-ol

Guidance literature:: Multi-step reaction with 5 steps

1.1: (-)-diisopinocampheylborane / tetrahydrofuran / 24 h / -23 °C

1.2: 95 percent / aq. NaOH; aq. H₂O₂ / 6 h / 20 °C

2.1: 94 percent / PCC / CH₂Cl₂ / 20 °C

3.1: 88 percent / m-CPBA; NaHCO₃ / CH₂Cl₂ / 10 h / 20 °C

4.1: 85 percent / LAH / tetrahydrofuran / 4 h / 0 - 20 °C

5.1: 73 percent / CSA / acetone / 3 h

With lithium aluminium tetrahydride; camphor-10-sulfonic acid; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; diisopinocampheylborane; pyridinium chlorochromate; In tetrahydrofuran; dichloromethane; acetone; 3.1: Baeyer-Villiger oxidation;
DOI:10.1016/j.tetlet.2004.06.121