(R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione

Base Information

Chemical Name:(R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione
CAS No.:173069-42-6
Molecular Formula:C₁₉H₂₉NO₄Si
Molecular Weight:363.529
Hs Code.:

Synonyms:(R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione

Suppliers and Price of (R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione

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 (R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione

There total 6 articles about (R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione 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: 95.0%

: 173069-36-8
(3S,4S)-1-benzyl-4-<(1S)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-3-hydroxy-4-methylazetidin-2-one

: 173069-42-6
(R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione

Guidance literature:: With sodium hypochlorite; 2,2,6,6-tetramethyl-piperidine-N-oxyl; In dichloromethane; water; at 0 ℃; for 0.0833333h;
DOI:10.1039/c39950002327

Reference yield: 90.0%

: 173069-39-1
(R)-1-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-azetidine-2,3-dione

: 173069-42-6
(R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at -40 ℃; for 2h;
DOI:10.1039/c39950002327

Reference yield:

: 167777-72-2
(-)-S-3-<oxy>-2-butanone

: 173069-42-6
(R)-3-Benzyl-4-[(S)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-oxazolidine-2,5-dione

Guidance literature:: Multi-step reaction with 5 steps

1: TiCl₄ / -78 °C

2: NEt₃ / CH₂Cl₂ / 20 h / -78 deg C to r.t.

3: NH₄HCO₃ / 10percent Pd-C / methanol

4: 88 percent / P₂O₅ / dimethylsulfoxide / 20 h / Ambient temperature

5: 90 percent / MCPBA / CH₂Cl₂ / 2 h / -40 °C

With phosphorus pentoxide; titanium tetrachloride; ammonium bicarbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In methanol; dichloromethane; dimethyl sulfoxide;
DOI:10.1039/c39950002327