(3R,4S,5S,6R)-6-[(R)-3-Methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-4-triethylsilanyloxy-tetrahydro-pyran-2-one

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Chemical Name:(3R,4S,5S,6R)-6-[(R)-3-Methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-4-triethylsilanyloxy-tetrahydro-pyran-2-one
CAS No.:647015-21-2
Molecular Formula:C₂₅H₄₂O₆Si
Molecular Weight:466.69
Hs Code.:

Synonyms:(3R,4S,5S,6R)-6-[(R)-3-Methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-4-triethylsilanyloxy-tetrahydro-pyran-2-one

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Chemical Property of (3R,4S,5S,6R)-6-[(R)-3-Methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-4-triethylsilanyloxy-tetrahydro-pyran-2-one

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Technology Process of (3R,4S,5S,6R)-6-[(R)-3-Methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-4-triethylsilanyloxy-tetrahydro-pyran-2-one

There total 3 articles about (3R,4S,5S,6R)-6-[(R)-3-Methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-4-triethylsilanyloxy-tetrahydro-pyran-2-one 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: 87.0%

: 79271-56-0
triethylsilyl trifluoromethyl sulfonate

: 647015-18-7
(3R,4S,5R,6R)-4-Hydroxy-6-[(R)-3-methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-tetrahydro-pyran-2-one

: 647015-21-2
(3R,4S,5S,6R)-6-[(R)-3-Methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-4-triethylsilanyloxy-tetrahydro-pyran-2-one

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane; at 25 ℃; for 2h;
DOI:10.1021/ja030496v

Reference yield:

: 400737-43-1
(2R,3S,4R,5R,7R)-5-(tert-Butyl-dimethyl-silanyloxy)-3-hydroxy-8-methoxy-7-(4-methoxy-benzyloxy)-2,4-dimethyl-octanoic acid methoxy-methyl-amide

: 647015-21-2
(3R,4S,5S,6R)-6-[(R)-3-Methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-4-triethylsilanyloxy-tetrahydro-pyran-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: TBAF / tetrahydrofuran / 12 h / 0 - 25 °C

2: 600 mg / TFA / tetrahydrofuran / 1 h / 0 °C

3: 87 percent / 2,6-lutidine / CH₂Cl₂ / 2 h / 25 °C

With 2,6-dimethylpyridine; tetrabutyl ammonium fluoride; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja030496v

Reference yield:

: 647015-17-6
(2R,3S,4S,5R,7R)-3,5-Dihydroxy-8-methoxy-7-(4-methoxy-benzyloxy)-2,4-dimethyl-octanoic acid methoxy-methyl-amide

: 647015-21-2
(3R,4S,5S,6R)-6-[(R)-3-Methoxy-2-(4-methoxy-benzyloxy)-propyl]-3,5-dimethyl-4-triethylsilanyloxy-tetrahydro-pyran-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 600 mg / TFA / tetrahydrofuran / 1 h / 0 °C

2: 87 percent / 2,6-lutidine / CH₂Cl₂ / 2 h / 25 °C

With 2,6-dimethylpyridine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja030496v