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(2R,3R,4aR,8S,8aS)-5-(benzyloxy)-2,3,8-trimethoxy-2,3-dimethylhexahydro-2H-pyrano[3,4-b][1,4]dioxine

Base Information Edit
  • Chemical Name:(2R,3R,4aR,8S,8aS)-5-(benzyloxy)-2,3,8-trimethoxy-2,3-dimethylhexahydro-2H-pyrano[3,4-b][1,4]dioxine
  • CAS No.:1449755-31-0
  • Molecular Formula:C19H28O7
  • Molecular Weight:368.427
  • Hs Code.:
  • Mol file:1449755-31-0.mol
(2R,3R,4aR,8S,8aS)-5-(benzyloxy)-2,3,8-trimethoxy-2,3-dimethylhexahydro-2H-pyrano[3,4-b][1,4]dioxine

Synonyms:(2R,3R,4aR,8S,8aS)-5-(benzyloxy)-2,3,8-trimethoxy-2,3-dimethylhexahydro-2H-pyrano[3,4-b][1,4]dioxine

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Chemical Property of (2R,3R,4aR,8S,8aS)-5-(benzyloxy)-2,3,8-trimethoxy-2,3-dimethylhexahydro-2H-pyrano[3,4-b][1,4]dioxine Edit
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Technology Process of (2R,3R,4aR,8S,8aS)-5-(benzyloxy)-2,3,8-trimethoxy-2,3-dimethylhexahydro-2H-pyrano[3,4-b][1,4]dioxine

There total 3 articles about (2R,3R,4aR,8S,8aS)-5-(benzyloxy)-2,3,8-trimethoxy-2,3-dimethylhexahydro-2H-pyrano[3,4-b][1,4]dioxine 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:
Guidance literature:
C18H26O7; With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.25h; Inert atmosphere;
methyl iodide; In tetrahydrofuran; at 0 ℃; for 8h; Inert atmosphere;
DOI:10.1016/j.tet.2013.07.009
Guidance literature:
Multi-step reaction with 3 steps
1.1: acetyl chloride / 0 °C
1.2: 120 h / 0 - 20 °C
2.1: trimethyl orthoformate / methanol / 12 h / Reflux
3.1: sodium hydride / tetrahydrofuran / 0.25 h / 0 °C / Inert atmosphere
3.2: 8 h / 0 °C / Inert atmosphere
With sodium hydride; acetyl chloride; trimethyl orthoformate; In tetrahydrofuran; methanol;
DOI:10.1016/j.tet.2013.07.009
Guidance literature:
Multi-step reaction with 2 steps
1.1: trimethyl orthoformate / methanol / 12 h / Reflux
2.1: sodium hydride / tetrahydrofuran / 0.25 h / 0 °C / Inert atmosphere
2.2: 8 h / 0 °C / Inert atmosphere
With sodium hydride; trimethyl orthoformate; In tetrahydrofuran; methanol;
DOI:10.1016/j.tet.2013.07.009
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