(2R,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate

Base Information

Chemical Name:(2R,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate
CAS No.:1400685-21-3
Molecular Formula:C₃₇H₄₃NO₃
Molecular Weight:549.753
Hs Code.:

Synonyms:(2R,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate

Suppliers and Price of (2R,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate

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,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate

There total 1 articles about (2R,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate 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:

: 128-39-2
2,6-di-tert-butylphenol

: benzyl 2-(4-(tert-butoxy)benzyl)but-2-enoate

: 17480-69-2
(S)-N-benzyl-1-phenylethylamine

: 1400685-21-3
(2R,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate

: (2S,3R)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate

Guidance literature:: (S)-N-benzyl-1-phenylethylamine; In toluene; at -78 - 0 ℃; for 0.25h; Inert atmosphere;

benzyl 2-(4-(tert-butoxy)benzyl)but-2-enoate; In toluene; at -78 - -30 ℃; for 3h; Inert atmosphere;

2,6-di-tert-butylphenol; In tetrahydrofuran; toluene; at -78 - 20 ℃; for 2h; Inert atmosphere;
DOI:10.1021/ja306311r

Reference yield:

: 1400685-21-3
(2R,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate

: C₁₅H₂₃NO₃

Guidance literature:: With palladium hydroxide, 20 wt% on carbon; ammonium formate; acetic acid; In methanol; Reflux; Inert atmosphere;
DOI:10.1021/ja306311r

Reference yield:

: 1400685-21-3
(2R,3S)-benzyl 3-(benzyl((S)-1-phenylethyl)amino-2-(4-tertbutoxy)benzyl)butanoate

: 1400685-23-5
(2R,3S)-3-amino-2-(4-(tert-butoxy)benzyl)butanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: palladium hydroxide, 20 wt% on carbon; ammonium formate; acetic acid / methanol / Reflux; Inert atmosphere

2: chloro-trimethyl-silane; N-ethyl-N,N-diisopropylamine / dichloromethane

With chloro-trimethyl-silane; palladium hydroxide, 20 wt% on carbon; ammonium formate; acetic acid; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;
DOI:10.1021/ja306311r