(5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-pyran-2-one

Base Information

• Chemical Name: (5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-pyran-2-one
• CAS No.: 924286-01-1
• Molecular Formula: C₂₅H₃₂O₃Si
• Molecular Weight: 408.613
• Mol file: 924286-01-1.mol

Synonyms:(5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-pyran-2-one

Chemical Property of (5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-pyran-2-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-pyran-2-one

There total 6 articles about (5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-pyran-2-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: 89.0%

(2S,3R,4S)-3-acryloxy-1-(tert-butyldiphenylsilyloxy)-2,4-dimethylhex-5-ene (924286-00-0) → (5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-pyran-2-one (924286-01-1)

Guidance literature:

With Grubbs catalyst first generation; In dichloromethane; at 40 ℃; for 12h;

DOI:10.3987/com-06-s(w)13

Reference yield:

(2S)-3-{[tert-butyl(diphenyl)silyl]oxy}-2-methylpropanal (92817-88-4) → (5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-pyran-2-one (924286-01-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 91 percent / iPr₂NEt / CH₂Cl₂ / 2 h / 25 °C

2: 89 percent / Grubbs' I catalyst / CH₂Cl₂ / 12 h / 40 °C

With N-ethyl-N,N-diisopropylamine; Grubbs catalyst first generation; In dichloromethane;

DOI:10.1021/ja066477d

Reference yield:

(R)-3-(tert-butyldiphenylsilyloxy)-2-methylpropan-1-ol (95514-04-8) → (5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-pyran-2-one (924286-01-1)

Guidance literature:

Multi-step reaction with 4 steps

1: 95 percent / NMO; TPAP; molecular sieves 4 Angstroem / CH₂Cl₂ / 0.5 h / 0 °C

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

3: 89 percent / Grubbs' I catalyst / CH₂Cl₂ / 12 h / 40 °C

With N-methyl-2-indolinone; tetrapropylammonium perruthennate; 4 A molecular sieve; N-ethyl-N,N-diisopropylamine; Grubbs catalyst first generation; In dichloromethane;

DOI:10.1021/ja066477d

upstream raw materials:

(2S,3R,4S)-3-acryloxy-1-(tert-butyldiphenylsilyloxy)-2,4-dimethylhex-5-ene

(2S)-3-{[tert-butyl(diphenyl)silyl]oxy}-2-methylpropanal

(R)-3-(tert-butyldiphenylsilyloxy)-2-methylpropan-1-ol

1-(tert-butyl-diphenyl-silanyloxy)-2(S),4(S)-dimethyl-hex-5-en-3(R)-ol

Downstream raw materials:

(5S,6R)-6-[(1S)-2-(tert-butyl-diphenylsilanyloxy)-1-methyl-ethyl]-5-methyl-5,6-dihydro-2H-pyran-2-ol

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

bis[(9H-fluoren-9-yl)methyl](2S,3S,6S)-1-(4-methoxybenzyloxy)-2-methyl-6-((2S,3S)-3-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)heptan-3-yl phosphate

(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