Acetic acid (2R,4aR,6S,7R,8R,8aR)-6-methoxy-2-phenyl-8-(tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester

Base Information

• Chemical Name: Acetic acid (2R,4aR,6S,7R,8R,8aR)-6-methoxy-2-phenyl-8-(tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester
• CAS No.: 107657-10-3
• Molecular Formula: C₂₁H₂₈O₈
• Molecular Weight: 408.449
• Mol file: 107657-10-3.mol

Synonyms:Acetic acid (2R,4aR,6S,7R,8R,8aR)-6-methoxy-2-phenyl-8-(tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester

Chemical Property of Acetic acid (2R,4aR,6S,7R,8R,8aR)-6-methoxy-2-phenyl-8-(tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of Acetic acid (2R,4aR,6S,7R,8R,8aR)-6-methoxy-2-phenyl-8-(tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester

There total 3 articles about Acetic acid (2R,4aR,6S,7R,8R,8aR)-6-methoxy-2-phenyl-8-(tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl 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: 91.0%

3,4-dihydro-2H-pyran (110-87-2) + Acetic acid (2R,4aR,6S,7R,8R,8aS)-8-hydroxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester (107657-09-0) → Acetic acid (2R,4aR,6S,7R,8R,8aR)-6-methoxy-2-phenyl-8-(tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester (107657-10-3)

Guidance literature:

toluene-4-sulfonic acid; In dichloromethane; at 0 ℃; for 0.5h;

DOI:10.1021/ja00243a043

Reference yield:

methyl 2-O-acetyl-4,6-O-benzylidene-α-D-glucopyranoside (2774-23-4,20750-02-1,25577-40-6,37180-49-7,37180-53-3,57538-70-2,96779-61-2,98392-36-0,107657-07-8,107657-09-0,130195-96-9,141611-58-7,144607-24-9,144607-27-2,150654-15-2,150654-16-3) → Acetic acid (2R,4aR,6S,7R,8R,8aR)-6-methoxy-2-phenyl-8-(tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester (107657-10-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 98 percent / PDC, 4 Angstroem MS / CH₂Cl₂ / 16 h / 25 °C

2: 96 percent / NaBH₄ / tetrahydrofuran; methanol / 0.02 h / -10 °C

3: 91 percent / TsOH / CH₂Cl₂ / 0.5 h / 0 °C

With sodium tetrahydroborate; dipyridinium dichromate; 4 Angstroem MS; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; dichloromethane;

DOI:10.1021/ja00243a043

Reference yield:

Acetic acid (2R,4aR,6S,7S,8aR)-6-methoxy-8-oxo-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester (107657-08-9) → Acetic acid (2R,4aR,6S,7R,8R,8aR)-6-methoxy-2-phenyl-8-(tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester (107657-10-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 96 percent / NaBH₄ / tetrahydrofuran; methanol / 0.02 h / -10 °C

2: 91 percent / TsOH / CH₂Cl₂ / 0.5 h / 0 °C

With sodium tetrahydroborate; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; dichloromethane;

DOI:10.1021/ja00243a043

upstream raw materials:

3,4-dihydro-2H-pyran

Acetic acid (2R,4aR,6S,7R,8R,8aS)-8-hydroxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester

methyl 2-O-acetyl-4,6-O-benzylidene-α-D-glucopyranoside

Acetic acid (2R,4aR,6S,7S,8aR)-6-methoxy-8-oxo-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester

Downstream raw materials:

3-azido-4-O-(tert-butyldimethylsilyl)-3,6-dideoxy-α-D-glucopyranose 1,2-diacetate