2-phenethyl-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)-5-(triisopropylsilyl)pent-4-ynamide

Base Information

Chemical Name:2-phenethyl-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)-5-(triisopropylsilyl)pent-4-ynamide
CAS No.:1425052-50-1
Molecular Formula:C₂₉H₃₄F₇NOSi
Molecular Weight:573.669
Hs Code.:

Synonyms:2-phenethyl-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)-5-(triisopropylsilyl)pent-4-ynamide

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Chemical Property of 2-phenethyl-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)-5-(triisopropylsilyl)pent-4-ynamide

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Technology Process of 2-phenethyl-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)-5-(triisopropylsilyl)pent-4-ynamide

There total 2 articles about 2-phenethyl-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)-5-(triisopropylsilyl)pent-4-ynamide 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: 80.0%

: 1425052-39-6
2-methyl-4-phenyl-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)butanamide

: 111409-79-1
1-bromo-2-(triisopropylsilyl)acetylene

: 1425052-50-1
2-phenethyl-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)-5-(triisopropylsilyl)pent-4-ynamide

Guidance literature:: With bis(η3-allyl-μ-chloropalladium(II)); C₂₃H₃₃N₂⁽¹⁺⁾*BF₄^(1-); caesium carbonate; In diethyl ether; at 20 - 85 ℃; for 8.08333h; Schlenk technique; Inert atmosphere;
DOI:10.1021/ja400648w

Reference yield:

: 1949-41-3
2-methyl-4-phenylbutanoic acid

: 651-83-2
4-trifluoromethyl-2,3,5,6-tetrafluoroaniline

: 1425052-50-1
2-phenethyl-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)-5-(triisopropylsilyl)pent-4-ynamide

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride / toluene / 12.5 h / 0 - 20 °C / Reflux; Inert atmosphere

2: bis(η3-allyl-μ-chloropalladium(II)); C23H33N2(1+)*BF4(1-); caesium carbonate / diethyl ether / 8.08 h / 20 - 85 °C / Schlenk technique; Inert atmosphere

With oxalyl dichloride; bis(η3-allyl-μ-chloropalladium(II)); C₂₃H₃₃N₂⁽¹⁺⁾*BF₄^(1-); caesium carbonate; In diethyl ether; toluene;
DOI:10.1021/ja400648w