2-(2,6-diethylphenyl)-4,4-dimethyl-5H-1,3-oxazole

Base Information

Chemical Name:2-(2,6-diethylphenyl)-4,4-dimethyl-5H-1,3-oxazole
CAS No.:66464-27-5
Molecular Formula:C15H21NO
Molecular Weight:231.338
Hs Code.:
DSSTox Substance ID:DTXSID001212957
Nikkaji Number:J2.274.610C

Synonyms:66464-27-5;DTXSID001212957;2-(2,6-Diethylphenyl)-4,5-dihydro-4,4-dimethyloxazole

Suppliers and Price of 2-(2,6-diethylphenyl)-4,4-dimethyl-5H-1,3-oxazole

Supply Marketing:

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

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Chemical Property of 2-(2,6-diethylphenyl)-4,4-dimethyl-5H-1,3-oxazole

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:231.162314293
Heavy Atom Count:17
Complexity:283

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1=C(C(=CC=C1)CC)C2=NC(CO2)(C)C

Technology Process of 2-(2,6-diethylphenyl)-4,4-dimethyl-5H-1,3-oxazole

There total 3 articles about 2-(2,6-diethylphenyl)-4,4-dimethyl-5H-1,3-oxazole 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: 74.0%

: 19312-06-2
4,5-dihydro-4,4-dimethyl-2-phenoxazole

: 597-64-8
tetraethyltin

: 66464-22-0
2-(2-ethylphenyl)-4,4-dimethyl-4,5-dihydrooxazole

: 66464-27-5
4,4-dimethyl-2-(2,6-diethylphenyl)oxazoline

Guidance literature:: With palladium diacetate; copper diacetate; p-benzoquinone; In acetonitrile; at 100 ℃; for 40h;
DOI:10.1021/ja0570943

Reference yield:

: 385-00-2
2,6-difluorobenzoic acid

: 66464-27-5
4,4-dimethyl-2-(2,6-diethylphenyl)oxazoline

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂

2: tetrahydrofuran / 65 °C

With thionyl chloride; In tetrahydrofuran;
DOI:10.1016/S0040-4039(01)85089-9