(1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6-dihydroxy-3-(thymin-1-yl)-7-(4-tolylsulfonyloxy)-2-oxabicyclo[3.3.0]octane

Base Information

Chemical Name:(1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6-dihydroxy-3-(thymin-1-yl)-7-(4-tolylsulfonyloxy)-2-oxabicyclo[3.3.0]octane
CAS No.:383191-83-1
Molecular Formula:C₃₃H₃₄N₂O₁₀S
Molecular Weight:650.706
Hs Code.:

Synonyms:(1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6-dihydroxy-3-(thymin-1-yl)-7-(4-tolylsulfonyloxy)-2-oxabicyclo[3.3.0]octane

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Chemical Property of (1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6-dihydroxy-3-(thymin-1-yl)-7-(4-tolylsulfonyloxy)-2-oxabicyclo[3.3.0]octane

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Technology Process of (1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6-dihydroxy-3-(thymin-1-yl)-7-(4-tolylsulfonyloxy)-2-oxabicyclo[3.3.0]octane

There total 4 articles about (1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6-dihydroxy-3-(thymin-1-yl)-7-(4-tolylsulfonyloxy)-2-oxabicyclo[3.3.0]octane 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: 77.0%

: 98-59-9
p-toluenesulfonyl chloride

: 383191-82-0
(1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6,7-trihydroxy-3-(thymin-1-yl)-2-oxabicyclo[3.3.0]octane

: 383191-83-1
(1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6-dihydroxy-3-(thymin-1-yl)-7-(4-tolylsulfonyloxy)-2-oxabicyclo[3.3.0]octane

Guidance literature:: With pyridine; at 20 ℃; for 48h;
DOI:10.1039/b104438a

Reference yield:

: 352422-92-5
(1R,3R,4R,5R,8R)-5,8-Bis(benzyloxy)-4-hydroxy-3-(thymin-1-yl)-2-oxabicyclo[3.3.0]oct-6-ene

: 383191-83-1
(1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6-dihydroxy-3-(thymin-1-yl)-7-(4-tolylsulfonyloxy)-2-oxabicyclo[3.3.0]octane

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / pyridine / 3 h / 20 °C

2: 85 percent / aq. NaOH / ethanol / 16 h / Heating

3: 83 percent / aq. OsO₄; N-methylmorpholine N-oxide / tetrahydrofuran; 2-methyl-propan-2-ol / 144 h / 50 °C

4: 77 percent / pyridine / 48 h / 20 °C

With pyridine; sodium hydroxide; osmium(VIII) oxide; 4-methylmorpholine N-oxide; In tetrahydrofuran; ethanol; tert-butyl alcohol;
DOI:10.1039/b104438a

Reference yield:

: 383191-81-9
(1R,3R,4S,5R,8R)-5,8-Bis(benzyloxy)-4-hydroxy-3-(thymin-1-yl)-2-oxabicyclo[3.3.0]oct-6-ene

: 383191-83-1
(1R,3R,4S,5R,6R,7R,8R)-5,8-Bis(benzyloxy)-4,6-dihydroxy-3-(thymin-1-yl)-7-(4-tolylsulfonyloxy)-2-oxabicyclo[3.3.0]octane

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / aq. OsO₄; N-methylmorpholine N-oxide / tetrahydrofuran; 2-methyl-propan-2-ol / 144 h / 50 °C

2: 77 percent / pyridine / 48 h / 20 °C

With pyridine; osmium(VIII) oxide; 4-methylmorpholine N-oxide; In tetrahydrofuran; tert-butyl alcohol;
DOI:10.1039/b104438a