(2R,4R,5R)-5-[3-(t-butyldimethylsilyloxy)propyl]-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane

Base Information

Chemical Name:(2R,4R,5R)-5-[3-(t-butyldimethylsilyloxy)propyl]-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane
CAS No.:854490-42-9
Molecular Formula:C₂₈H₄₂O₅Si
Molecular Weight:486.724
Hs Code.:

Synonyms:(2R,4R,5R)-5-[3-(t-butyldimethylsilyloxy)propyl]-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane

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Chemical Property of (2R,4R,5R)-5-[3-(t-butyldimethylsilyloxy)propyl]-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane

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Technology Process of (2R,4R,5R)-5-[3-(t-butyldimethylsilyloxy)propyl]-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane

There total 5 articles about (2R,4R,5R)-5-[3-(t-butyldimethylsilyloxy)propyl]-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane 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: 96.0%

: 854490-28-1
(2R,4R,5R)-5-(3-hydroxypropyl)-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane

: 18162-48-6
tert-butyldimethylsilyl chloride

: 854490-42-9
(2R,4R,5R)-5-[3-(t-butyldimethylsilyloxy)propyl]-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 0 ℃; for 3h;
DOI:10.1021/ol0507625

Reference yield:

: 854490-26-9
(2R,4R,5R)-4-hydroxymethyl-2-phenyl-5-(prop-2-enyl)-1,3-dioxane

: 854490-42-9
(2R,4R,5R)-5-[3-(t-butyldimethylsilyloxy)propyl]-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane

Guidance literature:: Multi-step reaction with 3 steps

1.1: 97 percent / NaH / dimethylformamide / 3.5 h / 0 °C

2.1: BH₃*SMe₂ complex / tetrahydrofuran / 2.5 h / 0 °C

2.2: 86 percent / NaOH; H₂O₂ / H₂O; tetrahydrofuran / 1 h / 0 °C

3.1: 96 percent / imidazole / dimethylformamide / 3 h / 0 °C

With 1H-imidazole; dimethylsulfide borane complex; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/ol0507625

Reference yield:

: 854490-27-0
(2R,4R,5R)-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-5-(prop-2-enyl)-1,3-dioxane

: 854490-42-9
(2R,4R,5R)-5-[3-(t-butyldimethylsilyloxy)propyl]-4-[(4-methoxybenzyloxy)methyl]-2-phenyl-1,3-dioxane

Guidance literature:: Multi-step reaction with 2 steps

1.1: BH₃*SMe₂ complex / tetrahydrofuran / 2.5 h / 0 °C

1.2: 86 percent / NaOH; H₂O₂ / H₂O; tetrahydrofuran / 1 h / 0 °C

2.1: 96 percent / imidazole / dimethylformamide / 3 h / 0 °C

With 1H-imidazole; dimethylsulfide borane complex; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/ol0507625