(2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester

Base Information

Chemical Name:(2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester
CAS No.:152033-18-6
Molecular Formula:C₂₂H₃₄N₂O₃
Molecular Weight:374.524
Hs Code.:

Synonyms:(2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester

Suppliers and Price of (2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester

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 (2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester

There total 1 articles about (2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester 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:

: 100-39-0
benzyl bromide

: 75-03-6
ethyl iodide

: 119838-44-7
tert-butoxycarbonyl-2-(tert-butyl)-3-methyl-4-oxo-1-imidazolidinecarboxylate

: 152033-18-6
(2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester

Guidance literature:: Yield given. Multistep reaction;

Reference yield: 82.0%

: 152033-18-6
(2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester

: (2R)-2-Ethyl-phenylalanin-(N-methylamid)

Guidance literature:: With hydrogenchloride; In methanol; Heating;

Reference yield:

: 152033-18-6
(2R,5R)-5-Benzyl-2-(t-butyl)-5-ethyl-3-methyl-4-oxo-1-imdazolidincarbonsaeure-t-butylester

: 132616-90-1
(R)-2-amino-2-ethyl-3-phenylpropionic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / 6N HCl / methanol / Heating

2: 82 percent / NEt₃, 4-(dimethylamino)pyridine / CH₂Cl₂ / 0 deg C to room temp.; 12 h at room temp.

3: 96 percent / 4 N HCl / dioxane / 4 h / 80 °C

4: 96 percent / conc. aq. HCl / 24 h / 100 °C

With hydrogenchloride; dmap; triethylamine; In 1,4-dioxane; methanol; dichloromethane;