(2R,2'RS,4RS)-7-benzyloxy-1-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)heptan-4-ol

Base Information

Chemical Name:(2R,2'RS,4RS)-7-benzyloxy-1-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)heptan-4-ol
CAS No.:251558-53-9
Molecular Formula:C₂₀H₂₉F₃O₄
Molecular Weight:390.443
Hs Code.:

Synonyms:(2R,2'RS,4RS)-7-benzyloxy-1-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)heptan-4-ol

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Chemical Property of (2R,2'RS,4RS)-7-benzyloxy-1-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)heptan-4-ol

Chemical Property:

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Technology Process of (2R,2'RS,4RS)-7-benzyloxy-1-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)heptan-4-ol

There total 4 articles about (2R,2'RS,4RS)-7-benzyloxy-1-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)heptan-4-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: 59.0%

: 5470-84-8
4-benzyloxybutanal

: 251558-45-9
(2RS,2'R)-2-[3-iodo-2-(trifluoromethyl)propoxy]tetrahydropyran

: 251558-53-9
(2R,2'RS,4RS)-7-benzyloxy-1-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)heptan-4-ol

Guidance literature:: With tert.-butyl lithium; In diethyl ether; pentane; at -105 - -78 ℃;

Reference yield:

: 110-87-2
3,4-dihydro-2H-pyran

: 251558-53-9
(2R,2'RS,4RS)-7-benzyloxy-1-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)heptan-4-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / pyridinium p-toluenesulfonate / CH₂Cl₂

2: 84 percent / DIBAH / diethyl ether / -40 - 0 °C

3: 83 percent / iodine; imidazole; triphenylphosphane / CH₂Cl₂ / 10 h / 20 °C

4: 59 percent / tBuLi / diethyl ether; pentane / -105 - -78 °C

With 1H-imidazole; iodine; tert.-butyl lithium; pyridinium p-toluenesulfonate; diisobutylaluminium hydride; triphenylphosphine; In diethyl ether; dichloromethane; pentane; 1: Etherification / 2: Reduction / 3: Iodination / 4: Alkylation;

Reference yield:

: 251558-43-7
(2R,2'RS)-3-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)propan-1-ol

: 251558-53-9
(2R,2'RS,4RS)-7-benzyloxy-1-(tetrahydropyran-2-yloxy)-2-(trifluoromethyl)heptan-4-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / iodine; imidazole; triphenylphosphane / CH₂Cl₂ / 10 h / 20 °C

2: 59 percent / tBuLi / diethyl ether; pentane / -105 - -78 °C

With 1H-imidazole; iodine; tert.-butyl lithium; triphenylphosphine; In diethyl ether; dichloromethane; pentane; 1: Iodination / 2: Alkylation;