(2R,6R)-2-(3-Benzyloxy-propyl)-6-((S)-5,5-dimethyl-2-oxo-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl)-3,6-dihydro-2H-pyran

Base Information

• Chemical Name: (2R,6R)-2-(3-Benzyloxy-propyl)-6-((S)-5,5-dimethyl-2-oxo-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl)-3,6-dihydro-2H-pyran
• CAS No.: 224947-58-4
• Molecular Formula: C₂₀H₂₈O₅S
• Molecular Weight: 380.505

Synonyms:(2R,6R)-2-(3-Benzyloxy-propyl)-6-((S)-5,5-dimethyl-2-oxo-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl)-3,6-dihydro-2H-pyran

Chemical Property of (2R,6R)-2-(3-Benzyloxy-propyl)-6-((S)-5,5-dimethyl-2-oxo-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl)-3,6-dihydro-2H-pyran

Chemical Property:

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Technology Process of (2R,6R)-2-(3-Benzyloxy-propyl)-6-((S)-5,5-dimethyl-2-oxo-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl)-3,6-dihydro-2H-pyran

There total 3 articles about (2R,6R)-2-(3-Benzyloxy-propyl)-6-((S)-5,5-dimethyl-2-oxo-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl)-3,6-dihydro-2H-pyran 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%

(S)-1-[(2R,6R)-6-(3-Benzyloxy-propyl)-5,6-dihydro-2H-pyran-2-yl]-3-methyl-butane-2,3-diol → (2R,6R)-2-(3-Benzyloxy-propyl)-6-((S)-5,5-dimethyl-2-oxo-2λ4-[1,3,2]dioxathiolan-4-ylmethyl)-3,6-dihydro-2H-pyran (224947-58-4)

Guidance literature:

With 1H-imidazole; thionyl chloride; In tetrahydrofuran; at -20 - 20 ℃;

DOI:10.1016/S0040-4039(99)00214-2

Reference yield:

[(2R,6R)-6-(3-Benzyloxy-propyl)-5,6-dihydro-2H-pyran-2-yl]-acetaldehyde (194423-23-9) → (2R,6R)-2-(3-Benzyloxy-propyl)-6-((S)-5,5-dimethyl-2-oxo-2λ4-[1,3,2]dioxathiolan-4-ylmethyl)-3,6-dihydro-2H-pyran (224947-58-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 40 percent / n-BuLi / diethyl ether / 0 °C

2: AD-mix-α, MeSO2NH2 / 2-methyl-propan-2-ol; H2O / 0 - 20 °C

3: 95 percent / SOCl₂, imidazole / tetrahydrofuran / -20 - 20 °C

With 1H-imidazole; AD-mix-α; n-butyllithium; thionyl chloride; methanesulfonamide; In tetrahydrofuran; diethyl ether; water; tert-butyl alcohol;

DOI:10.1016/S0040-4039(99)00214-2

Reference yield:

(2R,6R)-2-(3-Benzyloxy-propyl)-6-(3-methyl-but-2-enyl)-3,6-dihydro-2H-pyran (224947-56-2) → (2R,6R)-2-(3-Benzyloxy-propyl)-6-((S)-5,5-dimethyl-2-oxo-2λ4-[1,3,2]dioxathiolan-4-ylmethyl)-3,6-dihydro-2H-pyran (224947-58-4)

Guidance literature:

Multi-step reaction with 2 steps

1: AD-mix-α, MeSO2NH2 / 2-methyl-propan-2-ol; H2O / 0 - 20 °C

2: 95 percent / SOCl₂, imidazole / tetrahydrofuran / -20 - 20 °C

With 1H-imidazole; AD-mix-α; thionyl chloride; methanesulfonamide; In tetrahydrofuran; water; tert-butyl alcohol;

DOI:10.1016/S0040-4039(99)00214-2

upstream raw materials:

[(2R,6R)-6-(3-Benzyloxy-propyl)-5,6-dihydro-2H-pyran-2-yl]-acetaldehyde

(2R,6R)-2-(3-Benzyloxy-propyl)-6-(3-methyl-but-2-enyl)-3,6-dihydro-2H-pyran

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