3-tert-Butyl-1,3-oxazolidin-2-one

Base Information

• Chemical Name: 3-tert-Butyl-1,3-oxazolidin-2-one
• CAS No.: 40482-46-0
• Molecular Formula: C7H13NO2
• Molecular Weight: 0.00000
• DSSTox Substance ID: DTXSID301032136
• Nikkaji Number: J541.930A
• Mol file: 40482-46-0.mol

Synonyms:3-tert-Butyl-1,3-oxazolidin-2-one;40482-46-0;3-(tert-Butyl)oxazolidin-2-one;3-tert-Butyl-2-oxo-1,3-oxazolidine;3-tert-Butyl-2-oxazolidinone;SCHEMBL783215;3-tert-butyl-oxazolidin-2-one;DTXSID301032136;3-tert-Butyl-1,3-oxazolidin-2-one #

Chemical Property of 3-tert-Butyl-1,3-oxazolidin-2-one

Chemical Property:

• Vapor Pressure: 0.00814mmHg at 25°C
• PSA: 0.00000
• LogP: 0.00000
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 143.094628657
• Heavy Atom Count: 10
• Complexity: 148

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(C)(C)N1CCOC1=O

Technology Process of 3-tert-Butyl-1,3-oxazolidin-2-one

There total 3 articles about 3-tert-Butyl-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:

N-tert-butylaziridine (4017-38-3) + carbon dioxide (124-38-9,18923-20-1) → TMSO (40482-46-0)

Guidance literature:

With 1,3-bis(tert-butyl)-imidazolium-2-carboxylate; In isopropyl alcohol; at 90 ℃; for 20h; under 37503.8 Torr; Inert atmosphere; Autoclave;

DOI:10.1039/c2gc36414j

Reference yield:

tert-butyl-carbamic acid 2-chloro-ethyl ester (89796-59-8) → TMSO (40482-46-0)

Guidance literature:

With sodium ethanolate; In ethanol; at 65 - 70 ℃; for 1h;

DOI:10.1246/bcsj.35.1309

Reference yield:

→ TMSO (40482-46-0)

Guidance literature:

entspr. β-Aminoalkohol, Diethylcarbonat;

DOI:10.1007/BF01028454

upstream raw materials:

tert-butyl-carbamic acid 2-chloro-ethyl ester

N-tert-butylaziridine

carbon dioxide

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