3-Benzyl-1,3-oxazolidin-2-one

Base Information

• Chemical Name: 3-Benzyl-1,3-oxazolidin-2-one
• CAS No.: 2510-33-0
• Molecular Formula: C10H11NO2
• Molecular Weight: 177.203
• DSSTox Substance ID: DTXSID90440673
• Nikkaji Number: J498.399H,J3.091.461I
• Wikidata: Q82257040
• Mol file: 2510-33-0.mol

Synonyms:3-benzyl-1,3-oxazolidin-2-one;3-benzyloxazolidin-2-one;2510-33-0;benzyloxazolidinone;3-(Phenylmethyl)-2-oxazolidinone;benzyl-2-oxazolidinone;3-benzyl-oxazolidin-2-one;3beta-Benzyloxazolidine-2-one;SCHEMBL531434;DTXSID90440673;DBVTYDLZMXNRIN-UHFFFAOYSA-N;(S)-BENZYL-2-OXAZOLIDINONE

Chemical Property of 3-Benzyl-1,3-oxazolidin-2-one

Chemical Property:

• XLogP3: 1.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 177.078978594
• Heavy Atom Count: 13
• Complexity: 187

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1COC(=O)N1CC2=CC=CC=C2

Technology Process of 3-Benzyl-1,3-oxazolidin-2-one

There total 37 articles about 3-Benzyl-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: 96.0%

4-(trifluoromethoxy)benzonitrile (332-25-2) + N-Benzylethanolamine (104-63-2) → N-benzyl-2-oxazolidinone (2510-33-0) + benzonitrile (100-47-0)

Guidance literature:

With 3,7-di([1,1′-biphenyl]-4-yl)-10-(naphthalen-1-yl)-10H-phenoxazine; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 24h; Reagent/catalyst; Inert atmosphere; Irradiation; Schlenk technique;

DOI:10.1002/chem.201804603

Reference yield: 95.0%

1-benzylaziridine (1074-42-6) + carbon dioxide (124-38-9,18923-20-1) → N-benzyl-2-oxazolidinone (2510-33-0)

Guidance literature:

With DBN; lithium iodide; In toluene; at 50 ℃; for 24h; Inert atmosphere;

DOI:10.1016/j.tetlet.2011.09.092

Reference yield: 93.5%

carbon dioxide (124-38-9,18923-20-1) + ethylene dibromide (106-93-4) + benzylamine (100-46-9) → N-benzyl-2-oxazolidinone (2510-33-0)

Guidance literature:

With potassium phosphate; In N,N-dimethyl-formamide; at 130 ℃; for 10h; under 760.051 Torr;

upstream raw materials:

2-chloroethyl N-benzylcarbamate

Methyl trichloroacetate

N-Benzylethanolamine

Ethyl trichloroacetate

Downstream raw materials:

N-benzyl-2-chloroethan-1-amine

N-methyl-N-phenyl-N'-(phenylmethyl)-1,2-ethanediamine

N¹-benzyl-N²-phenylethane-1,2-diamine

benzyl[2-(phenylsulfanyl)ethyl]amine

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