(R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane

Base Information

Chemical Name:(R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane
CAS No.:252953-37-0
Molecular Formula:C₃₀H₄₅NO₅Si
Molecular Weight:527.777
Hs Code.:

Synonyms:(R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane

Suppliers and Price of (R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane

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)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane

There total 1 articles about (R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane 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: 85.0%

: 58479-61-1
tert-butylchlorodiphenylsilane

: 188476-24-6
2,2-Dimethyl-propionic acid (S)-2-tert-butoxycarbonylamino-3-hydroxy-2-methyl-propyl ester

: 252953-37-0
(R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 25 ℃; for 48h;
DOI:10.1021/jo990957o

Reference yield: 71.0%

: 252953-37-0
(R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane

: 252953-38-1
(R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-propanol

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; at -78 ℃;
DOI:10.1021/jo990957o

Reference yield:

: 252953-37-0
(R)-2-((tert-butoxycarbonyl)amino)-3-((tert-butyldiphenylsilyl)oxy)-2-methyl-1-(pivaloyloxy)propane

: 252953-39-2
(R)-N-(tert-butoxycarbonyl)-4-((tert-butyldiphenylsilyloxy)methyl)-2,2,4-trimethyloxazolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / DIBAL-H / CH₂Cl₂ / -78 °C

2: 94 percent / p-toluenesulfonic acid / toluene / Heating

With diisobutylaluminium hydride; toluene-4-sulfonic acid; In dichloromethane; toluene; 1: Reduction / 2: Cyclization;
DOI:10.1021/jo990957o