2-Oxazolidinone, 3-(4-chlorophenyl)-5-methyl-

Base Information

• Chemical Name: 2-Oxazolidinone, 3-(4-chlorophenyl)-5-methyl-
• CAS No.: 14423-08-6
• Molecular Formula: C₁₀H₁₀ClNO₂
• Molecular Weight: 211.648
• DSSTox Substance ID: DTXSID90465785
• Nikkaji Number: J302.707D

Synonyms:14423-08-6;2-Oxazolidinone, 3-(4-chlorophenyl)-5-methyl-;3-(4-chlorophenyl)-5-methyloxazolidin-2-one;SCHEMBL24794874;DTXSID90465785

Chemical Property of 2-Oxazolidinone, 3-(4-chlorophenyl)-5-methyl-

Chemical Property:

• XLogP3: 2.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 211.0400063
• Heavy Atom Count: 14
• Complexity: 226

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1CN(C(=O)O1)C2=CC=C(C=C2)Cl

Technology Process of 2-Oxazolidinone, 3-(4-chlorophenyl)-5-methyl-

There total 15 articles about 2-Oxazolidinone, 3-(4-chlorophenyl)-5-methyl- 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: 99.0%

carbon dioxide (124-38-9,18923-20-1) + 4-chloro-aniline (106-47-8) + methyloxirane (75-56-9,16033-71-9) → propylene glycol (57-55-6,63625-56-9) + 3-(4-chlorophenyl)-5-methyloxazolidin-2-one (14423-08-6,111609-86-0,111609-87-1)

Guidance literature:

With C₂₄H₂₅N₄O₃⁽¹⁺⁾*I^(1-); 1,8-diazabicyclo[5.4.0]undec-7-ene; at 90 ℃; for 4h; under 3750.38 Torr; Autoclave;

DOI:10.1039/c9ob00224c

Reference yield: 93.0%

p-chlorphenylisocyanate (104-12-1) + methyloxirane (75-56-9,16033-71-9) → 3-(4-chlorophenyl)-5-methyloxazolidin-2-one (14423-08-6,111609-86-0,111609-87-1)

Guidance literature:

With samarium (III) iodide; In tetrahydrofuran; at 20 ℃; for 3.5h;

Reference yield: 92.0%

→ 3-(4-chlorophenyl)-5-methyloxazolidin-2-one (14423-08-6,111609-86-0,111609-87-1)

Guidance literature:

With 3-butyl-1-methylimidazolium acetate; at 100 ℃; for 3h; Inert atmosphere; Green chemistry;

upstream raw materials:

p-chlorphenylisocyanate

methyloxirane

1,2-propylene cyclic carbonate

4-chloro-aniline

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