(Z)-2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-acrylic acid benzyl ester

Base Information

Chemical Name:(Z)-2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-acrylic acid benzyl ester
CAS No.:125718-59-4
Molecular Formula:C₂₁H₂₂N₂O₆
Molecular Weight:398.415
Hs Code.:

Synonyms:(Z)-2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-acrylic acid benzyl ester

Suppliers and Price of (Z)-2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-acrylic acid benzyl 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 (Z)-2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-acrylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (Z)-2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-acrylic acid benzyl ester

There total 2 articles about (Z)-2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-acrylic acid benzyl 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: 47.0%

: 636-98-6
p-nitrobenzene iodide

: 94882-75-4
benzyl (2-t-butoxycarbonylamino)acrylate

: 125718-59-4
(Z)-2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-acrylic acid benzyl ester

Guidance literature:: With tetrabutyl-ammonium chloride; sodium hydrogencarbonate; palladium diacetate; In N,N-dimethyl-formamide; at 85 ℃; for 40h;

Reference yield:

: 145612-59-5
2-t-butoxycarbonylamino-3-hydroxypropionic acid benzyl ester

: 125718-59-4
(Z)-2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-acrylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / NEt₃, MsCl / CH₂Cl₂ / 1.) 0-2 deg C, 15 min, 2.) room temp., 1 h

2: 47 percent / n-Bu₄NCl, NaHCO₃ / Pd(OAc)2 / dimethylformamide / 40 h / 85 °C

With tetrabutyl-ammonium chloride; sodium hydrogencarbonate; methanesulfonyl chloride; triethylamine; palladium diacetate; In dichloromethane; N,N-dimethyl-formamide;