3-[(4-Aminophenyl)methyl]-1,3-oxazolidin-2-one

Base Information

Chemical Name:3-[(4-Aminophenyl)methyl]-1,3-oxazolidin-2-one
CAS No.:99068-33-4
Molecular Formula:C₁₀H₁₂N₂O₂
Molecular Weight:192.217
Hs Code.:
European Community (EC) Number:864-465-9

Synonyms:3-[(4-aminophenyl)methyl]-1,3-oxazolidin-2-one;99068-33-4;3-(4-Amino-benzyl)-oxazolidin-2-one;SCHEMBL259624;WOIBIOHIFPYFSO-UHFFFAOYSA-N;3-(4-Aminobenzyl)oxazolidin-2-one;AKOS000211812;DB-135526;CS-0248922;EN300-41930;G27328;AB01002657-01;Z323040094;3-[(4-Aminophenyl)methyl]-1,3-oxazolidin-2-one, AldrichCPR

Suppliers and Price of 3-[(4-Aminophenyl)methyl]-1,3-oxazolidin-2-one

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
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price

Total 4 raw suppliers

Chemical Property of 3-[(4-Aminophenyl)methyl]-1,3-oxazolidin-2-one

Chemical Property:

XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:192.089877630
Heavy Atom Count:14
Complexity:212

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1COC(=O)N1CC2=CC=C(C=C2)N

Technology Process of 3-[(4-Aminophenyl)methyl]-1,3-oxazolidin-2-one

There total 1 articles about 3-[(4-Aminophenyl)methyl]-1,3-oxazolidin-2-one 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:

: 99072-36-3
3-(4-nitrobenzyl)oxazolidin-2-one

: 99068-33-4
3-(4-aminobenzyl)-1,3-oxazolidin-2-one

Guidance literature:: With ethanol; iron; acetic acid;
DOI:10.1021/ja01608a032

Reference yield: 74.0%

: 99068-33-4
3-(4-aminobenzyl)-1,3-oxazolidin-2-one

: 36980-80-0
ethyl 3-ethoxy-2-[(ethoxycarbonyl)carbamoyl]acrylate

: ethyl 2,4-dioxo-1-{4-[(2-oxo-1,3-oxazolidin-3-yl)methyl]phenyl}-1,2,3,4-tetrahydropyrimidine-5-carboxylate

Guidance literature:: 3-(4-aminobenzyl)-1,3-oxazolidin-2-one; ethyl 3-ethoxy-2-[(ethoxycarbonyl)carbamoyl]acrylate; In ethanol; for 0.5h; Reflux;

With potassium tert-butylate; In ethanol; at 20 - 60 ℃; for 20.5h;

Reference yield:

: 99068-33-4
3-(4-aminobenzyl)-1,3-oxazolidin-2-one

: ethyl 3-[2-methyl-3-(trifluoromethyl)benzyl]-2,4-dioxo-1-{4-[(2-oxo-1,3-oxazolidin-3-yl)methyl]phenyl}-1,2,3,4-tetrahydropyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: ethanol / 0.5 h / Reflux

1.2: 20.5 h / 20 - 60 °C

2.1: potassium carbonate; potassium iodide / acetonitrile / 16 h / 80 °C

With potassium carbonate; potassium iodide; In ethanol; acetonitrile;