(1R,2S,3R,4R,6R)-4-((1R,2S,3R,4R,5R)-3,4-Dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-6-hydroxymethyl-cyclohexane-1,2,3-triol

Base Information

Chemical Name:(1R,2S,3R,4R,6R)-4-((1R,2S,3R,4R,5R)-3,4-Dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-6-hydroxymethyl-cyclohexane-1,2,3-triol
CAS No.:104976-65-0
Molecular Formula:C₁₃H₂₂O₉
Molecular Weight:322.312
Hs Code.:

Synonyms:(1R,2S,3R,4R,6R)-4-((1R,2S,3R,4R,5R)-3,4-Dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-6-hydroxymethyl-cyclohexane-1,2,3-triol

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Chemical Property of (1R,2S,3R,4R,6R)-4-((1R,2S,3R,4R,5R)-3,4-Dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-6-hydroxymethyl-cyclohexane-1,2,3-triol

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Technology Process of (1R,2S,3R,4R,6R)-4-((1R,2S,3R,4R,5R)-3,4-Dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-6-hydroxymethyl-cyclohexane-1,2,3-triol

There total 8 articles about (1R,2S,3R,4R,6R)-4-((1R,2S,3R,4R,5R)-3,4-Dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-6-hydroxymethyl-cyclohexane-1,2,3-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:

: 104976-64-9
[(1R,2R,3S,4S,5R)-2,3,4-Tris-benzyloxy-5-((1R,2R,3S,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-cyclohexyl]-methanol

: 104976-65-0
(1R,2S,3R,4R,6R)-4-((1R,2S,3R,4R,5R)-3,4-Dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-6-hydroxymethyl-cyclohexane-1,2,3-triol

Guidance literature:: With hydrogen; acetic acid; palladium on activated charcoal; In methanol; for 24h; under 22501.8 Torr;

Reference yield:

: 104976-44-5
1,6-Anhydro-2,3-di-O-benzyl-4-O-<(trifluormethyl)sulfonyl>-β-D-galactopyranose

: 104976-65-0
(1R,2S,3R,4R,6R)-4-((1R,2S,3R,4R,5R)-3,4-Dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-6-hydroxymethyl-cyclohexane-1,2,3-triol

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) THF, HMPA, 30 min, 0 deg C; 2.) 12 h, room temp.

2: HCl / methanol / 6 h / Ambient temperature

3: H₂ / Raney Ni / dioxane / 2 h / Ambient temperature

4: H₂, AcOH / Pd/C (10percent) / methanol / 24 h / 22501.8 Torr

With hydrogenchloride; hydrogen; sodium hydride; acetic acid; palladium on activated charcoal; nickel; In 1,4-dioxane; methanol;

Reference yield:

: 104976-61-6
1L-(1,3/2,4)-2,3,4-Tri-O-benzyl-5-C-<(2-methoxyethoxy)methoxymethyl>-5-cyclohexen-1,2,3,4-tetrol

: 104976-65-0
(1R,2S,3R,4R,6R)-4-((1R,2S,3R,4R,5R)-3,4-Dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-6-hydroxymethyl-cyclohexane-1,2,3-triol

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) THF, HMPA, 30 min, 0 deg C; 2.) 12 h, room temp.

2: HCl / methanol / 6 h / Ambient temperature

3: H₂ / Raney Ni / dioxane / 2 h / Ambient temperature

4: H₂, AcOH / Pd/C (10percent) / methanol / 24 h / 22501.8 Torr

With hydrogenchloride; hydrogen; sodium hydride; acetic acid; palladium on activated charcoal; nickel; In 1,4-dioxane; methanol;