ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate

Base Information

Chemical Name:ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate
CAS No.:1432466-53-9
Molecular Formula:C₁₆H₂₃NO₅
Molecular Weight:309.362
Hs Code.:

Synonyms:ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate

Suppliers and Price of ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate

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 ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate

There total 9 articles about ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate 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: 97.0%

: 481054-47-1
(2R,3R)-ethyl 3-amino-2-hydroxy-3-phenylpropanoate

: 24424-99-5
di-tert-butyl dicarbonate

: 1432466-53-9
ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate

Guidance literature:: With Thiamine hydrochloride; In neat (no solvent); at 20 ℃; for 0.0833333h;
DOI:10.1080/00397911.2021.1994998

Reference yield: 65.0%

: 1432466-23-3
C₁₆H₂₁NO₅

: 1432466-53-9
ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate

Guidance literature:: C₁₆H₂₁NO₅; With [(R,R)-N-(2-amino-1,2-diphenylethyl)pentafluorobenzenesulfonamide]chloride(p-cymene)ruthenium (II); In N,N-dimethyl-formamide; for 0.166667h;

With formic acid; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 1h; Reagent/catalyst; Solvent; enantioselective reaction;
DOI:10.1016/j.tetlet.2013.07.100

Reference yield:

: 155396-71-7
tert-butyl N-(phenyl(phenylsulfonyl)methyl)carbamate

: 1432466-53-9
ethyl (2R,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-3-phenylpropanoate

Guidance literature:: Multi-step reaction with 4 steps

1: cesium fluoride / tetrahydrofuran / 12 h / 60 °C / Inert atmosphere

2: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 20 °C / Inert atmosphere

3: Oxone; sodium hydrogencarbonate / water; dichloromethane; acetone / 0 - 20 °C / Inert atmosphere

4: formic acid; triethylamine; C₄₂H₄₁ClN₂O₂RuS / N,N-dimethyl-formamide / 18 h / 20 °C / Inert atmosphere

With Oxone; formic acid; C₄₂H₄₁ClN₂O₂RuS; sodium hydrogencarbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; cesium fluoride; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile; 2: |Mannich Aminomethylation;
DOI:10.1021/ol4009206