6-O-(3,5-di-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-allofuranos-6-yl)-3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose

Base Information

Chemical Name:6-O-(3,5-di-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-allofuranos-6-yl)-3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose
CAS No.:668993-08-6
Molecular Formula:C₄₆H₅₄O₁₁
Molecular Weight:782.928
Hs Code.:

Synonyms:6-O-(3,5-di-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-allofuranos-6-yl)-3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose

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Chemical Property of 6-O-(3,5-di-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-allofuranos-6-yl)-3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose

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Technology Process of 6-O-(3,5-di-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-allofuranos-6-yl)-3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose

There total 7 articles about 6-O-(3,5-di-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-allofuranos-6-yl)-3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose 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: 89.0%

: 668993-05-3
3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose

: 668993-06-4
Trifluoro-methanesulfonic acid (R)-2-benzyloxy-2-((3aR,5R,6R,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl ester

: 668993-08-6
6-O-(3,5-di-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-allofuranos-6-yl)-3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose

Guidance literature:: 3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose; With sodium hydride; In tetrahydrofuran;

Trifluoro-methanesulfonic acid (R)-2-benzyloxy-2-((3aR,5R,6R,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl ester; In tetrahydrofuran; at 20 ℃; for 12h;
DOI:10.1039/b407468h

Reference yield:

: 57099-04-4
3-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose

: 668993-08-6
6-O-(3,5-di-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-allofuranos-6-yl)-3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose

Guidance literature:: Multi-step reaction with 5 steps

1.1: 94 percent / pyridine / 12 h / 20 °C

2.1: 68 percent / NaH / 1,2-dimethoxy-ethane / 12 h

3.1: 91 percent / tetrabutylammonium fluoride / tetrahydrofuran / 12 h / 20 °C

4.1: 80 percent / Et₃N / CH₂Cl₂ / -10 - 20 °C

5.1: NaH / tetrahydrofuran

5.2: 89 percent / tetrahydrofuran / 12 h / 20 °C

With pyridine; tetrabutyl ammonium fluoride; sodium hydride; triethylamine; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane;
DOI:10.1039/b407468h

Reference yield:

: 217089-45-7
3,5-di-O-benzyl-6-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-α-D-allofuranose

: 668993-08-6
6-O-(3,5-di-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-allofuranos-6-yl)-3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose

Guidance literature:: Multi-step reaction with 3 steps

1.1: 91 percent / tetrabutylammonium fluoride / tetrahydrofuran / 12 h / 20 °C

2.1: 80 percent / Et₃N / CH₂Cl₂ / -10 - 20 °C

3.1: NaH / tetrahydrofuran

3.2: 89 percent / tetrahydrofuran / 12 h / 20 °C

With tetrabutyl ammonium fluoride; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1039/b407468h