3-Benzyl-5-methyl-1,3-oxazolidine-2,4-dione

Base Information

• Chemical Name: 3-Benzyl-5-methyl-1,3-oxazolidine-2,4-dione
• CAS No.: 1016-31-5
• Molecular Formula: C₁₁H₁₁NO₃
• Molecular Weight: 205.213
• DSSTox Substance ID: DTXSID30693626
• ChEMBL ID: CHEMBL2029551
• Mol file: 1016-31-5.mol

Synonyms:1016-31-5;3-Benzyl-5-methyl-1,3-oxazolidine-2,4-dione;DTXSID30693626

Chemical Property of 3-Benzyl-5-methyl-1,3-oxazolidine-2,4-dione

Chemical Property:

• XLogP3: 1.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 205.07389321
• Heavy Atom Count: 15
• Complexity: 271

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1C(=O)N(C(=O)O1)CC2=CC=CC=C2

Technology Process of 3-Benzyl-5-methyl-1,3-oxazolidine-2,4-dione

There total 8 articles about 3-Benzyl-5-methyl-1,3-oxazolidine-2,4-dione 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: 81.0%

carbon dioxide (124-38-9,18923-20-1) + N-benzyl-O-tosyllactamide → 3-benzyl-5-methyl-1,3-oxazolidine-2,4-dione (79658-55-2,1016-31-5)

Guidance literature:

With 1,1,2,2-tetracarboethoxy-ethylene; tetraethylammonium perchlorate; In N,N-dimethyl-formamide; electrolysis, Hg cathode, Pt anode;

DOI:10.1016/0040-4020(95)00257-9

Reference yield: 55.0%

carbon dioxide (124-38-9,18923-20-1) + N-benzyl-2-bromopropanamide (6653-71-0) → 3-benzyl-5-methyl-1,3-oxazolidine-2,4-dione (79658-55-2,1016-31-5) + N-benzylpropanamide (10264-12-7) + methyl N-benzyl-2-methylmalonamate

Guidance literature:

With tetraethylammonium perchlorate; methyl iodide; In N,N-dimethyl-formamide; at 15 ℃; mercury catode;

Reference yield: 51.0%

ethyl 2-hydroxypropionate (97-64-3,2676-33-7) + benzyl isothiocyanate (3173-56-6) → 3-benzyl-5-methyl-1,3-oxazolidine-2,4-dione (79658-55-2,1016-31-5)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; Reflux;

DOI:10.1016/j.bmcl.2012.04.093

upstream raw materials:

carbon dioxide

N-benzyl-2-chloropropionamide

N-benzyl-2-bromopropanamide

benzyl chloride

Downstream raw materials:

3-benzyl-5,5-dimethyloxazolidine-2,4-dione

N-(benzyl)-4,5-dimethyl-4-oxazolin-2-one