Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester

Base Information

Chemical Name:Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester
CAS No.:294842-99-2
Molecular Formula:C₂₂H₂₈NO₇P
Molecular Weight:449.441
Hs Code.:

Synonyms:Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester

Suppliers and Price of Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester

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 Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester

There total 4 articles about Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester 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: 58.0%

: 98-88-4
benzoyl chloride

: 294842-97-0
dimethyl (1R,2R)-2-[(tert-butoxycarbonyl)amino]-1-hydroxy-2-phenylethylphosphonate

: 294842-99-2
Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester

Guidance literature:: With dmap; triethylamine;
DOI:10.1016/S0957-4166(00)00203-2

Reference yield:

: 140196-38-9
1,1-dimethyl (2-oxo-1-phenylethyl)carbamate

: 294842-99-2
Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 51 percent / Et₃N / 24 h / 20 °C

2: 39 percent / DCC; DMAP / CH₂Cl₂ / 24 h / 20 °C

3: 94 percent / 25 percent aq. NH₄OH / tetrahydrofuran / 2 h / 20 °C

4: 58 percent / Et₃N; DMAP

With dmap; ammonium hydroxide; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; 1: Addition / 2: Esterification / 3: deesterification / 4: benzoylation;
DOI:10.1016/S0957-4166(00)00203-2

Reference yield:

: dimethyl (1S*,2S*)-2-[(tert-butoxycarbonyl)amino]-1-hydroxy-2-phenylethylphosphonate

: 294842-99-2
Benzoic acid (1R,2R)-2-tert-butoxycarbonylamino-1-(dimethoxy-phosphoryl)-2-phenyl-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 39 percent / DCC; DMAP / CH₂Cl₂ / 24 h / 20 °C

2: 94 percent / 25 percent aq. NH₄OH / tetrahydrofuran / 2 h / 20 °C

3: 58 percent / Et₃N; DMAP

With dmap; ammonium hydroxide; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; 1: Esterification / 2: deesterification / 3: benzoylation;
DOI:10.1016/S0957-4166(00)00203-2