2-({4-[3-(trifluoromethyl)diazirin-3-yl]phenyl}carbonyl)-4-[2-(trimethylsilyl)ethynyl]aniline

Base Information

Chemical Name:2-({4-[3-(trifluoromethyl)diazirin-3-yl]phenyl}carbonyl)-4-[2-(trimethylsilyl)ethynyl]aniline
CAS No.:1299312-81-4
Molecular Formula:C₂₀H₁₈F₃N₃OSi
Molecular Weight:401.463
Hs Code.:

Synonyms:2-({4-[3-(trifluoromethyl)diazirin-3-yl]phenyl}carbonyl)-4-[2-(trimethylsilyl)ethynyl]aniline

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Chemical Property of 2-({4-[3-(trifluoromethyl)diazirin-3-yl]phenyl}carbonyl)-4-[2-(trimethylsilyl)ethynyl]aniline

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Technology Process of 2-({4-[3-(trifluoromethyl)diazirin-3-yl]phenyl}carbonyl)-4-[2-(trimethylsilyl)ethynyl]aniline

There total 5 articles about 2-({4-[3-(trifluoromethyl)diazirin-3-yl]phenyl}carbonyl)-4-[2-(trimethylsilyl)ethynyl]aniline 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: 97.0%

: 1299312-79-0
2-({4-[3-(trifluoromethyl)diaziridin-3-yI]phenyl}carbonyl)-4-[2-(trimethyisilyl)ethynyl]aniline

: 1299312-81-4
2-({4-[3-(trifluoromethyl)diazirin-3-yl]phenyl}carbonyl)-4-[2-(trimethylsilyl)ethynyl]aniline

Guidance literature:: With manganese(IV) oxide; In diethyl ether; at 20 ℃; for 30h;

Reference yield:

: 1066-54-2
trimethylsilylacetylene

: 1299312-81-4
2-({4-[3-(trifluoromethyl)diazirin-3-yl]phenyl}carbonyl)-4-[2-(trimethylsilyl)ethynyl]aniline

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 0.33 h / 20 °C / Inert atmosphere; Darkness

2.1: 4-methyl-morpholine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 0.17 h / 20 °C

2.2: 16 h / 20 °C

3.1: n-butyllithium / tetrahydrofuran; hexanes / 2 h / -80 °C / Inert atmosphere; Cooling with ether-dry ice

4.1: manganese(IV) oxide / diethyl ether / 30 h / 20 °C

With 4-methyl-morpholine; manganese(IV) oxide; n-butyllithium; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; hexanes; diethyl ether; N,N-dimethyl-formamide;

Reference yield:

: 5326-47-6
2-amino-5-iodobenzoic acid

: 1299312-81-4
2-({4-[3-(trifluoromethyl)diazirin-3-yl]phenyl}carbonyl)-4-[2-(trimethylsilyl)ethynyl]aniline

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 0.33 h / 20 °C / Inert atmosphere; Darkness

2.1: 4-methyl-morpholine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 0.17 h / 20 °C

2.2: 16 h / 20 °C

3.1: n-butyllithium / tetrahydrofuran; hexanes / 2 h / -80 °C / Inert atmosphere; Cooling with ether-dry ice

4.1: manganese(IV) oxide / diethyl ether / 30 h / 20 °C

With 4-methyl-morpholine; manganese(IV) oxide; n-butyllithium; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; hexanes; diethyl ether; N,N-dimethyl-formamide;