(2S,3S,6R)-2-[(2S,5S,6R)-5-triethylsilyloxy-7-(4-methoxybenzyloxy)-6-methylheptan-2-yl]-6-methoxy-3-methyl-3,6-dihydro-2H-pyran

Base Information

• Chemical Name: (2S,3S,6R)-2-[(2S,5S,6R)-5-triethylsilyloxy-7-(4-methoxybenzyloxy)-6-methylheptan-2-yl]-6-methoxy-3-methyl-3,6-dihydro-2H-pyran
• CAS No.: 924286-49-7
• Molecular Formula: C₂₉H₅₀O₅Si
• Molecular Weight: 506.798
• Mol file: 924286-49-7.mol

Synonyms:(2S,3S,6R)-2-[(2S,5S,6R)-5-triethylsilyloxy-7-(4-methoxybenzyloxy)-6-methylheptan-2-yl]-6-methoxy-3-methyl-3,6-dihydro-2H-pyran

Chemical Property of (2S,3S,6R)-2-[(2S,5S,6R)-5-triethylsilyloxy-7-(4-methoxybenzyloxy)-6-methylheptan-2-yl]-6-methoxy-3-methyl-3,6-dihydro-2H-pyran

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2S,3S,6R)-2-[(2S,5S,6R)-5-triethylsilyloxy-7-(4-methoxybenzyloxy)-6-methylheptan-2-yl]-6-methoxy-3-methyl-3,6-dihydro-2H-pyran

There total 8 articles about (2S,3S,6R)-2-[(2S,5S,6R)-5-triethylsilyloxy-7-(4-methoxybenzyloxy)-6-methylheptan-2-yl]-6-methoxy-3-methyl-3,6-dihydro-2H-pyran 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:

(2S,3R,4S)-3-acryloxy-1-(tert-butyldiphenylsilyloxy)-2,4-dimethylhex-5-ene (924286-00-0) → (2S,3S,6R)-2-[(2S,5S,6R)-5-triethylsilyloxy-7-(4-methoxybenzyloxy)-6-methylheptan-2-yl]-6-methoxy-3-methyl-3,6-dihydro-2H-pyran (924286-49-7)

Guidance literature:

Multi-step reaction with 7 steps

1.1: 89 percent / Grubbs' I catalyst / CH₂Cl₂ / 12 h / 40 °C

2.1: DIBAL-H / CH₂Cl₂; toluene / 1 h / -78 °C

2.2: PPTS / 0.17 h / 25 °C

3.1: nBu₄NF / tetrahydrofuran / 12 h / 25 °C

4.1: NaH / benzene / 0.75 h

4.2: 5.50 g / benzene / 3 h / 25 °C

5.1: 90 percent / NaI / acetone / 12 h / 56 °C

6.1: t-BuLi / diethyl ether; pentane / 0.08 h / -78 °C

6.2: (2-Th)CuCNLi / diethyl ether; pentane / 0.08 h / -78 - 0 °C

6.3: diethyl ether; pentane / 1 h / 0 °C

7.1: 87 percent / imidazole / dimethylformamide / 1 h / 25 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; tert.-butyl lithium; sodium hydride; diisobutylaluminium hydride; sodium iodide; Grubbs catalyst first generation; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetone; toluene; pentane; benzene;

DOI:10.1021/ja066477d

Reference yield:

1-(tert-butyl-diphenyl-silanyloxy)-2(S),4(S)-dimethyl-hex-5-en-3(R)-ol (106357-26-0) → (2S,3S,6R)-2-[(2S,5S,6R)-5-triethylsilyloxy-7-(4-methoxybenzyloxy)-6-methylheptan-2-yl]-6-methoxy-3-methyl-3,6-dihydro-2H-pyran (924286-49-7)

Guidance literature:

Multi-step reaction with 8 steps

1.1: 91 percent / iPr₂NEt / CH₂Cl₂ / 2 h / 25 °C

2.1: 89 percent / Grubbs' I catalyst / CH₂Cl₂ / 12 h / 40 °C

3.1: DIBAL-H / CH₂Cl₂; toluene / 1 h / -78 °C

3.2: PPTS / 0.17 h / 25 °C

4.1: nBu₄NF / tetrahydrofuran / 12 h / 25 °C

5.1: NaH / benzene / 0.75 h

5.2: 5.50 g / benzene / 3 h / 25 °C

6.1: 90 percent / NaI / acetone / 12 h / 56 °C

7.1: t-BuLi / diethyl ether; pentane / 0.08 h / -78 °C

7.2: (2-Th)CuCNLi / diethyl ether; pentane / 0.08 h / -78 - 0 °C

7.3: diethyl ether; pentane / 1 h / 0 °C

8.1: 87 percent / imidazole / dimethylformamide / 1 h / 25 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; tert.-butyl lithium; sodium hydride; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; sodium iodide; Grubbs catalyst first generation; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetone; toluene; pentane; benzene;

DOI:10.1021/ja066477d

Reference yield:

(2R,5S,6S)-6-[(1S)-2-iodo-1-methylethyl]-5-methyl-2-methoxy-5,6-dihydro-2H-pyran (924286-04-4) → (2S,3S,6R)-2-[(2S,5S,6R)-5-triethylsilyloxy-7-(4-methoxybenzyloxy)-6-methylheptan-2-yl]-6-methoxy-3-methyl-3,6-dihydro-2H-pyran (924286-49-7)

Guidance literature:

Multi-step reaction with 2 steps

1.1: t-BuLi / diethyl ether; pentane / 0.08 h / -78 °C

1.2: (2-Th)CuCNLi / diethyl ether; pentane / 0.08 h / -78 - 0 °C

1.3: diethyl ether; pentane / 1 h / 0 °C

2.1: 87 percent / imidazole / dimethylformamide / 1 h / 25 °C

With 1H-imidazole; tert.-butyl lithium; In diethyl ether; N,N-dimethyl-formamide; pentane;

DOI:10.1021/ja066477d

upstream raw materials:

2-(6-methoxy-3-methyl-3,6-dihydro-2H-pyran-2-yl)-propan-1-ol

(2R,5S,6S)-6-[(1S)-2-iodo-1-methylethyl]-5-methyl-2-methoxy-5,6-dihydro-2H-pyran

(2R,5S,6S)-6-[(1S)-2-(p-toluenesulfonyl)-1-methylethyl]-5-methyl-2-methoxy-5,6-dihydro-2H-pyran

(2R,5S,6S)-6-[(1S)-2-(tert-butyldiphenylsilyloxy)-1-methylethyl]-5-methyl-2-methoxy-5,6-dihydro-2H-pyran