(R)-1-[(3aR,5R,6S,6aR)-6-(2-Allyloxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol

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Chemical Name:(R)-1-[(3aR,5R,6S,6aR)-6-(2-Allyloxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol
CAS No.:319917-52-7
Molecular Formula:C₁₉H₂₆O₇
Molecular Weight:366.411
Hs Code.:

Synonyms:(R)-1-[(3aR,5R,6S,6aR)-6-(2-Allyloxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol

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Chemical Property of (R)-1-[(3aR,5R,6S,6aR)-6-(2-Allyloxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol

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Technology Process of (R)-1-[(3aR,5R,6S,6aR)-6-(2-Allyloxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol

There total 3 articles about (R)-1-[(3aR,5R,6S,6aR)-6-(2-Allyloxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol 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: 83.0%

: 3-O-(2-allyloxy benzyl)-1,2:5,6-diisopropylidene-α-D-glucofuranose

: 319917-52-7
(R)-1-[(3aR,5R,6S,6aR)-6-(2-Allyloxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol

Guidance literature:: With acetic acid; at 20 ℃; for 14h;
DOI:10.1016/S0040-4020(00)00844-9

Reference yield:

: 582-52-5
1,2:5,6-diacetone-D-glucose

: 319917-52-7
(R)-1-[(3aR,5R,6S,6aR)-6-(2-Allyloxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / Bu₄NBr / CH₂Cl₂; aq. NaOH / 4 h / 25 °C

2: 83 percent / aq. AcOH / 14 h / 20 °C

With tetrabutylammomium bromide; acetic acid; In sodium hydroxide; dichloromethane; 1: Alkylation / 2: Hydrolysis;
DOI:10.1016/S0040-4020(00)00844-9

Reference yield:

: 319918-15-5
1-(bromomethyl)-2-(prop-2-en-1-yloxy)benzene

: 319917-52-7
(R)-1-[(3aR,5R,6S,6aR)-6-(2-Allyloxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / Bu₄NBr / CH₂Cl₂; aq. NaOH / 4 h / 25 °C

2: 83 percent / aq. AcOH / 14 h / 20 °C

With tetrabutylammomium bromide; acetic acid; In sodium hydroxide; dichloromethane; 1: Alkylation / 2: Hydrolysis;
DOI:10.1016/S0040-4020(00)00844-9