(4aR,6R,7R,8R,8aS)-8-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

Base Information

Chemical Name:(4aR,6R,7R,8R,8aS)-8-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol
CAS No.:127874-01-5
Molecular Formula:C₁₉H₂₆O₇
Molecular Weight:366.411
Hs Code.:

Synonyms:(4aR,6R,7R,8R,8aS)-8-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

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Chemical Property of (4aR,6R,7R,8R,8aS)-8-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

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Technology Process of (4aR,6R,7R,8R,8aS)-8-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

There total 5 articles about (4aR,6R,7R,8R,8aS)-8-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 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: 46.0%

: 106-95-6
allyl bromide

: 127874-00-4
2-methoxyethyl 4,6-O-benzylidene-β-D-galactopyranoside

: (4aR,6R,7R,8S,8aS)-7,8-Bis-allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine

: (4aR,6R,7R,8S,8aR)-7-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-ol

: 127874-01-5
(4aR,6R,7R,8R,8aS)-8-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

Guidance literature:: With potassium hydroxide; In 1,2-dimethoxyethane; at 70 ℃; for 1.5h;
DOI:10.1246/bcsj.62.3549

Reference yield:

: 10257-28-0
D-Galactose

: 127874-01-5
(4aR,6R,7R,8R,8aS)-8-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 2.) Ag₂CO₃ / 1.) 25 deg C, 1.5 h, 2.) RT

2: 58 percent / NaOMe / methanol

3: 71 percent / ZnCl₂

4: 46 percent / KOH / 1,2-dimethoxy-ethane / 1.5 h / 70 °C

With potassium hydroxide; sodium methylate; silver carbonate; zinc(II) chloride; In methanol; 1,2-dimethoxyethane;
DOI:10.1246/bcsj.62.3549

Reference yield:

: 53144-52-8
2-methoxyethyl β-D-galactopyranoside

: 127874-01-5
(4aR,6R,7R,8R,8aS)-8-Allyloxy-6-(2-methoxy-ethoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / ZnCl₂

2: 46 percent / KOH / 1,2-dimethoxy-ethane / 1.5 h / 70 °C

With potassium hydroxide; zinc(II) chloride; In 1,2-dimethoxyethane;
DOI:10.1246/bcsj.62.3549