(2S,3R,5R)-5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexan-1-ol

Base Information

Chemical Name:(2S,3R,5R)-5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexan-1-ol
CAS No.:250346-42-0
Molecular Formula:C₂₅H₄₈O₄Si₂
Molecular Weight:468.825
Hs Code.:

Synonyms:(2S,3R,5R)-5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexan-1-ol

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Chemical Property of (2S,3R,5R)-5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexan-1-ol

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Technology Process of (2S,3R,5R)-5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexan-1-ol

There total 7 articles about (2S,3R,5R)-5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexan-1-ol 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: 82.0%

: 250346-41-9
(4R,2'R,3'R,5'R)-3-[5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexanoyl]-4-(phenylmethyl)oxazolidin-2-one

: 250346-42-0
(2S,3R,5R)-5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexan-1-ol

Guidance literature:: With lithium borohydride; In tetrahydrofuran; at 0 - 20 ℃; for 5h;
DOI:10.1039/a909243i

Reference yield:

: 250346-38-4
(4R,2'R,3'R,5'R)-3-[5-(tert-Butyldimethylsilyloxy)-3-hydroxy-2-(phenylmethoxy)hexanoyl]-4-(phenylmethyl)oxazolidin-2-one

: 250346-42-0
(2S,3R,5R)-5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / imidazole / dimethylformamide

2: 82 percent / lithium borohydride / tetrahydrofuran / 0 °C

With 1H-imidazole; lithium borohydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/ol991020c

Reference yield:

: 137238-71-2
(4R)-3-[2-(Phenylmethoxy)acetyl]-4-(phenylmethyl)oxazolidin-2-one

: 250346-42-0
(2S,3R,5R)-5-(tert-Butyldimethylsilyloxy)-2-(phenylmethoxy)-3-(triethylsilyloxy)hexan-1-ol

Guidance literature:: Multi-step reaction with 3 steps

1.1: tin(II) trifluoromethanesulfonate; triethylamine / CH₂Cl₂ / -78 °C

1.2: TMEDA / CH₂Cl₂ / cooling

2.1: 84 percent / imidazole / dimethylformamide

3.1: 82 percent / lithium borohydride / tetrahydrofuran / 0 °C

With 1H-imidazole; lithium borohydride; tin(II) trifluoromethanesulfonate; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol991020c