Trifluoro-methanesulfonic acid (1R,2S,3S,4R,5S,6R)-2,3-bis-benzyloxy-4,5-dihydroxy-6-methoxy-cyclohexyl ester

Base Information

Chemical Name:Trifluoro-methanesulfonic acid (1R,2S,3S,4R,5S,6R)-2,3-bis-benzyloxy-4,5-dihydroxy-6-methoxy-cyclohexyl ester
CAS No.:186382-60-5
Molecular Formula:C₂₂H₂₅F₃O₈S
Molecular Weight:506.497
Hs Code.:

Synonyms:Trifluoro-methanesulfonic acid (1R,2S,3S,4R,5S,6R)-2,3-bis-benzyloxy-4,5-dihydroxy-6-methoxy-cyclohexyl ester

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Chemical Property of Trifluoro-methanesulfonic acid (1R,2S,3S,4R,5S,6R)-2,3-bis-benzyloxy-4,5-dihydroxy-6-methoxy-cyclohexyl ester

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Technology Process of Trifluoro-methanesulfonic acid (1R,2S,3S,4R,5S,6R)-2,3-bis-benzyloxy-4,5-dihydroxy-6-methoxy-cyclohexyl ester

There total 2 articles about Trifluoro-methanesulfonic acid (1R,2S,3S,4R,5S,6R)-2,3-bis-benzyloxy-4,5-dihydroxy-6-methoxy-cyclohexyl ester 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:

: 186382-59-2
1D-(1,2,3,4)-1,2-di-O-benzyl-4-O-methylcyclohex-5-ene-1,2,3,4-tetraol

: 186382-60-5
Trifluoro-methanesulfonic acid (1R,2S,3S,4R,5S,6R)-2,3-bis-benzyloxy-4,5-dihydroxy-6-methoxy-cyclohexyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / CH₂Cl₂ / 0.5 h / 0 °C

2: aq. OsO₄, Me₃NO / acetone; 2-methyl-propan-2-ol / 48 h

With pyridine; osmium(VIII) oxide; trimethylamine-N-oxide; In dichloromethane; acetone; tert-butyl alcohol;
DOI:10.1016/S0957-4166(96)00461-2

Reference yield:

: (1S,2S,5S,6R)-5,6-Bis-benzyloxy-2-methoxy-3-tributylstannanyl-cyclohex-3-enol

: 186382-60-5
Trifluoro-methanesulfonic acid (1R,2S,3S,4R,5S,6R)-2,3-bis-benzyloxy-4,5-dihydroxy-6-methoxy-cyclohexyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 79 percent / NaOMe / methanol / 4 h / 60 °C

2: pyridine / CH₂Cl₂ / 0.5 h / 0 °C

3: aq. OsO₄, Me₃NO / acetone; 2-methyl-propan-2-ol / 48 h

With pyridine; osmium(VIII) oxide; trimethylamine-N-oxide; sodium methylate; In methanol; dichloromethane; acetone; tert-butyl alcohol;
DOI:10.1016/S0957-4166(96)00461-2