tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate

Base Information

Chemical Name:tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate
CAS No.:1338473-87-2
Molecular Formula:C₂₂H₁₉Cl₄F₃N₂O₃
Molecular Weight:558.212
Hs Code.:

Synonyms:tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate

Suppliers and Price of tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate

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 tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate

There total 6 articles about tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate 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: 76.0%

: 864736-87-8
1,2,3-trichloro-5-(1,1,1-trifluoroprop-2-en-2-yl)benzene

: 1338473-86-1
tert-butyl {2-chloro-5-[(E/Z)-chloro(hydroxyimino)methyl]benzyl}-carbamate

: 1338473-87-2
tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate

Guidance literature:: With sodium hydrogencarbonate; In N,N-dimethyl-formamide; at 20 ℃; for 24h;

Reference yield:

: 862248-93-9
(3,4,5-trichlorophenyl)boronic acid

: 1338473-87-2
tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / bis-triphenylphosphine-palladium(II) chloride / water; tetrahydrofuran / Reflux

2: sodium hydrogencarbonate / N,N-dimethyl-formamide / 24 h / 20 °C

With sodium hydrogencarbonate; potassium carbonate; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; water; N,N-dimethyl-formamide;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1338473-87-2
tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / dichloromethane / 24 h / 0 - 20 °C

2.1: n-butyllithium / tetrahydrofuran; hexanes / 0.42 h / -78 °C / Inert atmosphere

2.2: 2 h / 20 °C

3.1: hydroxylamine hydrochloride; sodium acetate / ethanol / 4 h / 20 °C

4.1: N-chloro-succinimide / N,N-dimethyl-formamide / 12 h / 20 °C

5.1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 24 h / 20 °C

With N-chloro-succinimide; n-butyllithium; hydroxylamine hydrochloride; sodium acetate; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; hexanes; ethanol; dichloromethane; N,N-dimethyl-formamide;