[(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane

Base Information

Chemical Name:[(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane
CAS No.:438002-56-3
Molecular Formula:C₄₆H₆₄O₈Si
Molecular Weight:773.095
Hs Code.:

[(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane

Synonyms:[(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane

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Chemical Property of [(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane

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Technology Process of [(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane

There total 12 articles about [(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane 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:

: 125901-90-8
(2R,3S)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol

: 370885-74-8
(R)-3-Benzyloxy-3-((2S,3R,5S,6R)-5-benzyloxy-6-benzyloxymethyl-2-methyl-3-triisopropylsilanyloxy-tetrahydro-pyran-2-yl)-propionaldehyde

: 438002-56-3
[(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane

Guidance literature:: With scandium tris(trifluoromethanesulfonate); In benzene; at 20 ℃; for 31.5h;
DOI:10.1021/jo010974p

Reference yield:

: 13154-24-0
triisopropylsilyl chloride

: 438002-56-3
[(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane

Guidance literature:: Multi-step reaction with 10 steps

1.1: 2,6-lutidine / CH₂Cl₂ / 14 h / 20 °C

2.1: p-toluenesulfonic acid hydrate / methanol; CH₂Cl₂ / 19.5 h / 20 °C

3.1: NaH / dimethylformamide / 0.25 h / 20 °C

3.2: 35.53 g / dimethylformamide / 16 h / 20 °C

4.1: 5.53 g / aq. OsO₄; N-methylmorpholine N-oxide / acetone / 19 h / 20 °C

5.1: NaIO₄ / tetrahydrofuran; H₂O / 9 h / 20 °C

6.1: 5.24 g / MgBr₂*Et₂O / CH₂Cl₂ / 2 h / -78 - 20 °C

7.1: NaH / dimethylformamide / 0.5 h / 20 °C

7.2: 100 percent / dimethylformamide / 4.5 h / 0 °C

8.1: osmiumm tetraxide; N-methylmorpholine N-oxide / acetone; H₂O / 9 h / 20 °C

9.1: NaIO₄ / tetrahydrofuran; H₂O / 1 h / 20 °C

10.1: 2.60 g / scandium trifluoromethanesulfonate / benzene / 31.5 h / 20 °C

With 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide; sodium hydride; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; magnesium bromide; scandium tris(trifluoromethanesulfonate); In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1021/jo010974p

Reference yield:

: 131310-61-7
(2R,4aR,6S,7R,8aS)-6-Methyl-2-phenyl-6-vinyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

: 438002-56-3
[(2S,3R,5S,6R)-5-Benzyloxy-6-benzyloxymethyl-2-((R)-1-benzyloxy-2-(2R,4aR,8aS)-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-2-yl-ethyl)-2-methyl-tetrahydro-pyran-3-yloxy]-triisopropyl-silane

Guidance literature:: Multi-step reaction with 10 steps

1.1: 2,6-lutidine / CH₂Cl₂ / 14 h / 20 °C

2.1: p-toluenesulfonic acid hydrate / methanol; CH₂Cl₂ / 19.5 h / 20 °C

3.1: NaH / dimethylformamide / 0.25 h / 20 °C

3.2: 35.53 g / dimethylformamide / 16 h / 20 °C

4.1: 5.53 g / aq. OsO₄; N-methylmorpholine N-oxide / acetone / 19 h / 20 °C

5.1: NaIO₄ / tetrahydrofuran; H₂O / 9 h / 20 °C

6.1: 5.24 g / MgBr₂*Et₂O / CH₂Cl₂ / 2 h / -78 - 20 °C

7.1: NaH / dimethylformamide / 0.5 h / 20 °C

7.2: 100 percent / dimethylformamide / 4.5 h / 0 °C

8.1: osmiumm tetraxide; N-methylmorpholine N-oxide / acetone; H₂O / 9 h / 20 °C

9.1: NaIO₄ / tetrahydrofuran; H₂O / 1 h / 20 °C

10.1: 2.60 g / scandium trifluoromethanesulfonate / benzene / 31.5 h / 20 °C

With 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide; sodium hydride; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; magnesium bromide; scandium tris(trifluoromethanesulfonate); In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1021/jo010974p