(2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-1-ol

Base Information

Chemical Name:(2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-1-ol
CAS No.:398478-23-4
Molecular Formula:C₂₆H₄₆O₆Si
Molecular Weight:482.733
Hs Code.:

Synonyms:(2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-1-ol

Suppliers and Price of (2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-1-ol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-1-ol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-1-ol

There total 7 articles about (2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-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: 91.0%

: (2S)-N-[(2S,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptanoyl]bornane-10,2-sultam

: 398478-23-4
(2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-1-ol

Guidance literature:: With lithium triethylborohydride; In tetrahydrofuran; at 20 ℃; for 3h;
DOI:10.1021/ja0177713

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 398478-23-4
(2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-1-ol

Guidance literature:: Multi-step reaction with 6 steps

1.1: 94 percent / imidazole; DMAP / dimethylformamide / 16 h / 20 °C

2.1: 21 g / OsO₄; NMO / acetone; 2-methyl-propan-2-ol / 16 h / 0 - 20 °C

3.1: 18.0 g / NaIO₄ / CH₂Cl₂ / 2 h / 20 °C

4.1: TiCl₄; i-Pr₂NEt / CH₂Cl₂ / 1 h / -78 °C

4.2: 92 percent / CH₂Cl₂ / 2 h / -78 °C

5.1: 91 percent / NaI; i-Pr₂NEt / 1,2-dimethoxy-ethane / 12 h / Heating

6.1: 91 percent / LiEt₃BH / tetrahydrofuran / 3 h / 20 °C

With 1H-imidazole; dmap; sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; titanium tetrachloride; lithium triethylborohydride; N-ethyl-N,N-diisopropylamine; sodium iodide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; N,N-dimethyl-formamide; acetone; tert-butyl alcohol;
DOI:10.1021/ja0177713

Reference yield:

: 380909-94-4
(3S)-1-[(4-methoxyphenyl)methoxy]hex-5-en-3-ol

: 398478-23-4
(2R,3R,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxybenzyloxy)-3-methoxymethoxy-2-(prop-2-enyl)heptan-1-ol

Guidance literature:: Multi-step reaction with 6 steps

1.1: 94 percent / imidazole; DMAP / dimethylformamide / 16 h / 20 °C

2.1: 21 g / OsO₄; NMO / acetone; 2-methyl-propan-2-ol / 16 h / 0 - 20 °C

3.1: 18.0 g / NaIO₄ / CH₂Cl₂ / 2 h / 20 °C

4.1: TiCl₄; i-Pr₂NEt / CH₂Cl₂ / 1 h / -78 °C

4.2: 92 percent / CH₂Cl₂ / 2 h / -78 °C

5.1: 91 percent / NaI; i-Pr₂NEt / 1,2-dimethoxy-ethane / 12 h / Heating

6.1: 91 percent / LiEt₃BH / tetrahydrofuran / 3 h / 20 °C

With 1H-imidazole; dmap; sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; titanium tetrachloride; lithium triethylborohydride; N-ethyl-N,N-diisopropylamine; sodium iodide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; N,N-dimethyl-formamide; acetone; tert-butyl alcohol;
DOI:10.1021/ja0177713