dodecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(dodecyloxycarbonyl)methyl]-α-D-glucopyranoside

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Chemical Name:dodecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(dodecyloxycarbonyl)methyl]-α-D-glucopyranoside
CAS No.:1295578-48-1
Molecular Formula:C₅₃H₈₀O₇
Molecular Weight:829.214
Hs Code.:

Synonyms:dodecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(dodecyloxycarbonyl)methyl]-α-D-glucopyranoside

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Chemical Property of dodecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(dodecyloxycarbonyl)methyl]-α-D-glucopyranoside

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Technology Process of dodecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(dodecyloxycarbonyl)methyl]-α-D-glucopyranoside

There total 2 articles about dodecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(dodecyloxycarbonyl)methyl]-α-D-glucopyranoside 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: 56.0%

: 112-53-8
1-dodecyl alcohol

: 1124225-72-4
(3aR,4R,5S,6R,7aR)-4,5-bis(benzyloxy)-6-benzyloxymethyl-2-oxohexahydrofuro[2,3-b]pyran

: 1295578-48-1
dodecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(dodecyloxycarbonyl)methyl]-α-D-glucopyranoside

Guidance literature:: (3aR,4R,5S,6R,7aR)-4,5-bis(benzyloxy)-6-benzyloxymethyl-2-oxohexahydrofuro[2,3-b]pyran; With calcium sulfate; scandium tris(trifluoromethanesulfonate); In dichloromethane; at 0 ℃; for 0.5h; Inert atmosphere;

1-dodecyl alcohol; In dichloromethane; at 0 - 20 ℃; stereoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2011.01.069

Reference yield:

: 946512-97-6
methyl 3,4,6-tri-O-benzyl-2-deoxy-2-C-[(bis-methoxycarbonyl)methyl]-β-D-glucopyranoside

: 1295578-48-1
dodecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(dodecyloxycarbonyl)methyl]-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hydroxide monohydrate / methanol; water / 1 h / Inert atmosphere; Reflux

2.1: acetic acid / toluene / 1 h / 110 °C / pH 3 - 4 / Inert atmosphere

3.1: calcium sulfate; scandium tris(trifluoromethanesulfonate) / dichloromethane / 0.5 h / 0 °C / Inert atmosphere

3.2: 0 - 20 °C / Inert atmosphere

With calcium sulfate; lithium hydroxide monohydrate; acetic acid; scandium tris(trifluoromethanesulfonate); In methanol; dichloromethane; water; toluene;
DOI:10.1016/j.tet.2011.01.069