(1R,2R,3R,5R,9R,10R,12S)-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.0^3,10.0^5,9>pentadecan-14-one

Base Information

• Chemical Name: (1R,2R,3R,5R,9R,10R,12S)-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.0^3,10.0^5,9>pentadecan-14-one
• CAS No.: 138034-50-1
• Molecular Formula: C₂₉H₃₆O₆Si
• Molecular Weight: 508.687

Synonyms:(1R,2R,3R,5R,9R,10R,12S)-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.0^3,10.0^5,9>pentadecan-14-one

Chemical Property of (1R,2R,3R,5R,9R,10R,12S)-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.0^3,10.0^5,9>pentadecan-14-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

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Technology Process of (1R,2R,3R,5R,9R,10R,12S)-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.0^3,10.0^5,9>pentadecan-14-one

There total 3 articles about (1R,2R,3R,5R,9R,10R,12S)-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.0^3,10.0^5,9>pentadecan-14-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: 73.0%

(1R,2R,3R,5R,9R,10R,12S,14RS)-14-ethoxy-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.03,10.05,9>pentadecane (138034-49-8,138127-43-2) → (1R,2R,3R,5R,9R,10R,12S)-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.03,10.05,9>pentadecan-14-one (138034-50-1)

Guidance literature:

With jones reagent; In acetone; at 0 ℃; for 2.5h;

DOI:10.1016/S0040-4020(01)89728-3

Reference yield:

(1R,5R,9R,10S,12S,14RS)-14-ethoxy-7,7-dimethyl-4,6,8,13-tetraoxatetracyclo<10.3.0.03,10.05,9>pentadec-2-ene (612501-92-5) → (1R,2R,3R,5R,9R,10R,12S)-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.03,10.05,9>pentadecan-14-one (138034-50-1)

Guidance literature:

Multi-step reaction with 3 steps

2: 68 percent / imidazole / dimethylformamide / 13 h / 55 °C

3: 73 percent / Jones reagent / acetone / 2.5 h / 0 °C

With 1H-imidazole; jones reagent; In N,N-dimethyl-formamide; acetone;

DOI:10.1016/S0040-4020(01)89728-3

Reference yield:

(1R,2R,3R,5R,9R,10R,12S,14RS)-14-ethoxy-7,7-dimethyl-4,6,8,13-tetraoxatetracyclo<10.3.0.03,10.05,9>pentadecan-2-ol (138034-47-6,138127-39-6,138127-41-0,138127-42-1) → (1R,2R,3R,5R,9R,10R,12S)-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.03,10.05,9>pentadecan-14-one (138034-50-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 68 percent / imidazole / dimethylformamide / 13 h / 55 °C

2: 73 percent / Jones reagent / acetone / 2.5 h / 0 °C

With 1H-imidazole; jones reagent; In N,N-dimethyl-formamide; acetone;

DOI:10.1016/S0040-4020(01)89728-3

upstream raw materials:

(1R,2R,3R,5R,9R,10R,12S,14RS)-14-ethoxy-7,7-dimethyl-2-(tert-butyldiphenylsilyloxy)-4,6,8,13-tetraoxatetracyclo<10.3.0.0^3,10.0^5,9>pentadecane

(1R,5R,9R,10S,12S,14RS)-14-ethoxy-7,7-dimethyl-4,6,8,13-tetraoxatetracyclo<10.3.0.0^3,10.0^5,9>pentadec-2-ene

(1R,2R,3R,5R,9R,10R,12S,14RS)-14-ethoxy-7,7-dimethyl-4,6,8,13-tetraoxatetracyclo<10.3.0.0^3,10.0^5,9>pentadecan-2-ol

Downstream raw materials:

(3aS,4R,4aR,7R,7aS,8aS)-4-(tert-Butyl-diphenyl-silanyloxy)-6,7-dihydroxy-octahydro-benzo[1,2-b;4,5-b']difuran-2-one

(3aS,4S,7aS)-4-(tert-Butyl-diphenyl-silanyloxy)-2-oxo-2,3,3a,4,7,7a-hexahydro-benzofuran-6-carbaldehyde

(1S,2S,6S)-4-hydroxymethyl-2-(tert-butyldiphenylsilyloxy)-7-oxabicyclo<4.3.0>non-3-en-8-one

Formic acid (3aS,4R,5R,6R,7aS)-4-(tert-butyl-diphenyl-silanyloxy)-6-formyl-2-oxo-octahydro-benzofuran-5-yl ester

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