<4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone

Base Information

Chemical Name:<4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone
CAS No.:126788-90-7
Molecular Formula:C₂₀H₂₁NO₅
Molecular Weight:355.39
Hs Code.:

Synonyms:<4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone

Suppliers and Price of <4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone

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 <4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of <4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone

There total 2 articles about <4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone 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:

: 88920-24-5
p-methoxybenzyloxy acetic acid

: 126788-90-7
<4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / diethyl ether / 1.58 h / -78 - 0 °C

2: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 10 min, 2.) a) ether, -70 deg C, 45 min, b) 0 deg C, 6 h

With n-butyllithium; triethylamine; In diethyl ether;
DOI:10.1021/ja00175a038

Reference yield:

: 77943-39-6
4-methyl-5-phenyloxazolidin-2-one

: 318514-55-5
C₁₅H₂₀O₅

: 126788-90-7
<4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone

Guidance literature:: With n-butyllithium; Yield given. Multistep reaction; 1.) THF, hexane, -78 deg C, 10 min, 2.) a) ether, -70 deg C, 45 min, b) 0 deg C, 6 h;
DOI:10.1021/ja00175a038

Reference yield: 88.0%

: 126788-90-7
<4R,5S>-3-<1-oxo-2-<(4-methoxyphenyl)methoxy>ethyl>-4-methyl-5-phenyl-2-oxazolidinone

: 148933-49-7
(E)-(2R,5S,7S)-9-Iodo-7-methoxy-2,8-dimethyl-5-triisopropylsilanyloxy-non-8-enal

: 148933-50-0
(4R,5S)-3-[(E)-(2R,3S,4R,7S,9S)-3-Hydroxy-11-iodo-9-methoxy-2-(4-methoxy-benzyloxy)-4,10-dimethyl-7-triisopropylsilanyloxy-undec-10-enoyl]-4-methyl-5-phenyl-oxazolidin-2-one

Guidance literature:: With di-n-butylboryl trifluoromethanesulfonate; triethylamine; In dichloromethane; toluene; at -50 - 0 ℃; for 1.5h;
DOI:10.1039/c39930000617