2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline

Base Information

Chemical Name:2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline
CAS No.:125290-74-6
Molecular Formula:C₁₅H₂₀F₃NOSi
Molecular Weight:315.411
Hs Code.:

Synonyms:2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline

Suppliers and Price of 2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline

There total 4 articles about 2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline 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:

: 446-17-3
2,4,5-trifluorobenzoic acid

: 125290-74-6
2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline

Guidance literature:: Multi-step reaction with 5 steps

1: COCl₂, DMF / CH₂Cl₂ / Ambient temperature

2: CH₂Cl₂ / Ambient temperature

3: SOCl₂ / CHCl₃ / Ambient temperature

4: 1) lithium diisopropylamide / 1) THF, -78 deg C, 30 min, 2) up to room temp.

5: 1) lithium diisopropylamide / 1) THF, 0 deg C, 30 min, 2) up to room temp.

With thionyl chloride; N,N-dimethyl-formamide; lithium diisopropyl amide; In dichloromethane; chloroform;
DOI:10.1002/jhet.5570270616

Reference yield:

: 88419-56-1
2,4,5-trifluorobenzoyl chloride

: 125290-74-6
2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline

Guidance literature:: Multi-step reaction with 4 steps

1: CH₂Cl₂ / Ambient temperature

2: SOCl₂ / CHCl₃ / Ambient temperature

3: 1) lithium diisopropylamide / 1) THF, -78 deg C, 30 min, 2) up to room temp.

4: 1) lithium diisopropylamide / 1) THF, 0 deg C, 30 min, 2) up to room temp.

With thionyl chloride; lithium diisopropyl amide; In dichloromethane; chloroform;
DOI:10.1002/jhet.5570270616

Reference yield:

: 2,4,5-Trifluoro-benzoic acid 2-amino-2-methyl-propyl ester

: 125290-74-6
2-<2,4,5-trifluoro-6-methyl-3-(trimethylsilyl)phenyl>-4,4-dimethyl-2-oxazoline

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂ / CHCl₃ / Ambient temperature

2: 1) lithium diisopropylamide / 1) THF, -78 deg C, 30 min, 2) up to room temp.

3: 1) lithium diisopropylamide / 1) THF, 0 deg C, 30 min, 2) up to room temp.

With thionyl chloride; lithium diisopropyl amide; In chloroform;
DOI:10.1002/jhet.5570270616