3-(2-Phenoxyacetyl)-1,3-oxazolidin-2-one

Base Information

Chemical Name:3-(2-Phenoxyacetyl)-1,3-oxazolidin-2-one
CAS No.:22445-79-0
Molecular Formula:C11H11NO4
Molecular Weight:221.213
Hs Code.:
DSSTox Substance ID:DTXSID401293767
Nikkaji Number:J905.746C

Synonyms:22445-79-0;DTXSID401293767;3-(2-Phenoxyacetyl)-2-oxazolidinone

Suppliers and Price of 3-(2-Phenoxyacetyl)-1,3-oxazolidin-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-(2-Phenoxyacetyl)-1,3-oxazolidin-2-one

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:221.06880783
Heavy Atom Count:16
Complexity:273

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1COC(=O)N1C(=O)COC2=CC=CC=C2

Technology Process of 3-(2-Phenoxyacetyl)-1,3-oxazolidin-2-one

There total 4 articles about 3-(2-Phenoxyacetyl)-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:

: 124-38-9,18923-20-1
carbon dioxide

: 194935-57-4
N-(2-bromoethyl)-2-phenoxyacetamide

: 22445-79-0
3-(2-phenoxyacetyl)oxazolidin-2-one

Guidance literature:: With oxygen; tetraethylammonium perchlorate; Yield given. Multistep reaction; 1.) -1.0 V vs SCE, MeCN, 2.) room temperature, overnight;
DOI:10.1021/jo970308h

Reference yield:

: 1943-83-5
2-chloroethyl isothiocyanate

: 701-99-5
Phenoxyacetyl chloride

: 22445-79-0
3-(2-phenoxyacetyl)oxazolidin-2-one

Guidance literature:: With N,N,N,N,N,N-hexamethylphosphoric triamide; bis(tri-n-butyltin)oxide; Yield given. Multistep reaction; 1.) 40 deg C, 1 h; 2.) r.t., 10 min;
DOI:10.1246/bcsj.62.853