(3R,3aS,6R,6aR)-6-(allyloxy)-3-[(4-methylphenyl)sulfonyloxy]hexahydrofuro[3,2-b]furan

Base Information

Chemical Name:(3R,3aS,6R,6aR)-6-(allyloxy)-3-[(4-methylphenyl)sulfonyloxy]hexahydrofuro[3,2-b]furan
CAS No.:853016-71-4
Molecular Formula:C₁₆H₂₀O₆S
Molecular Weight:340.397
Hs Code.:

Synonyms:(3R,3aS,6R,6aR)-6-(allyloxy)-3-[(4-methylphenyl)sulfonyloxy]hexahydrofuro[3,2-b]furan

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Chemical Property of (3R,3aS,6R,6aR)-6-(allyloxy)-3-[(4-methylphenyl)sulfonyloxy]hexahydrofuro[3,2-b]furan

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Technology Process of (3R,3aS,6R,6aR)-6-(allyloxy)-3-[(4-methylphenyl)sulfonyloxy]hexahydrofuro[3,2-b]furan

There total 3 articles about (3R,3aS,6R,6aR)-6-(allyloxy)-3-[(4-methylphenyl)sulfonyloxy]hexahydrofuro[3,2-b]furan 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: 85.0%

: 106-95-6
allyl bromide

: 72631-59-5
(3R,3aS,6R,6aR)-6-hydroxy-3-(4-methoxyphenyl)sulfonyloxyperhydrofuro[3,2-b]furan

: 853016-71-4
(3R,3aS,6R,6aR)-6-(allyloxy)-3-[(4-methylphenyl)sulfonyloxy]hexahydrofuro[3,2-b]furan

Guidance literature:: With potassium hydroxide; tetrabutylammomium bromide; In dichloromethane; water; at 20 ℃; for 6h;
DOI:10.1016/j.tet.2005.02.010

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 853016-71-4
(3R,3aS,6R,6aR)-6-(allyloxy)-3-[(4-methylphenyl)sulfonyloxy]hexahydrofuro[3,2-b]furan

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / pyridine / CH₂Cl₂ / 10 h / 20 °C

2: 85 percent / KOH; tetrabutylammonium bromide / H₂O; CH₂Cl₂ / 6 h / 20 °C

With pyridine; potassium hydroxide; tetrabutylammomium bromide; In dichloromethane; water;
DOI:10.1016/j.tet.2005.02.010

Reference yield:

: 641-74-7
1,4:3,6-dianhydro-D-mannitol

: 853016-71-4
(3R,3aS,6R,6aR)-6-(allyloxy)-3-[(4-methylphenyl)sulfonyloxy]hexahydrofuro[3,2-b]furan

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / pyridine / CH₂Cl₂ / 10 h / 20 °C

2: 85 percent / KOH; tetrabutylammonium bromide / H₂O; CH₂Cl₂ / 6 h / 20 °C

With pyridine; potassium hydroxide; tetrabutylammomium bromide; In dichloromethane; water;
DOI:10.1016/j.tet.2005.02.010