(1S,2S,3S,4R,5S)-5-(4-chloro-3-(phenoxymethyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol

Base Information

Chemical Name:(1S,2S,3S,4R,5S)-5-(4-chloro-3-(phenoxymethyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol
CAS No.:1416165-43-9
Molecular Formula:C₂₀H₂₁ClO₇
Molecular Weight:408.836
Hs Code.:

Synonyms:(1S,2S,3S,4R,5S)-5-(4-chloro-3-(phenoxymethyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol

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Chemical Property of (1S,2S,3S,4R,5S)-5-(4-chloro-3-(phenoxymethyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol

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Technology Process of (1S,2S,3S,4R,5S)-5-(4-chloro-3-(phenoxymethyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol

There total 4 articles about (1S,2S,3S,4R,5S)-5-(4-chloro-3-(phenoxymethyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-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: 100.0%

: 1416165-41-7
(2S,3R,4S,5S)-2-(4-chloro-3-(phenoxymethyl)phenyl)-6,6-bis(hydroxymethyl)-2-methoxytetrahydro-2H-pyran-3,4,5-triol

: 1416165-43-9
(1S,2S,3S,4R,5S)-5-(4-chloro-3-(phenoxymethyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;

Reference yield:

: 1416165-38-2
((2R,3R,4S,5R,6S)-6-(4-chloro-3-(phenoxymethyl)phenyl)-6-methoxy-3,4,5-tris((trimethylsilyl)oxy)tetrahydro-2H-pyran-2-yl)methanol

: 1416165-43-9
(1S,2S,3S,4R,5S)-5-(4-chloro-3-(phenoxymethyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; sulfur trioxide pyridine complex / dichloromethane; dimethyl sulfoxide / 3 h / 0 - 10 °C / Inert atmosphere

2: sodium ethanolate / ethanol / 55 °C / Inert atmosphere

3: trifluoroacetic acid / dichloromethane / 0 - 20 °C / Inert atmosphere

With sodium ethanolate; sulfur trioxide pyridine complex; triethylamine; trifluoroacetic acid; In ethanol; dichloromethane; dimethyl sulfoxide;

Reference yield:

: 1416165-40-6
(2S,3R,4S,5R,6S)-6-(4-chloro-3-(phenoxymethyl)phenyl)-6-methoxy-3,4,5-tris((trimethylsilyl)oxy)tetrahydro-2H-pyran-2-carbaldehyde

: 1416165-43-9
(1S,2S,3S,4R,5S)-5-(4-chloro-3-(phenoxymethyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol

Guidance literature:: Multi-step reaction with 2 steps

1: sodium ethanolate / ethanol / 55 °C / Inert atmosphere

2: trifluoroacetic acid / dichloromethane / 0 - 20 °C / Inert atmosphere

With sodium ethanolate; trifluoroacetic acid; In ethanol; dichloromethane;