tert-butyl (1R)-1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate

Base Information

Chemical Name:tert-butyl (1R)-1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate
CAS No.:845829-93-8
Molecular Formula:C₁₉H₂₉BFNO₄
Molecular Weight:365.253
Hs Code.:

Synonyms:tert-butyl (1R)-1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate

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Chemical Property of tert-butyl (1R)-1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate

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Technology Process of tert-butyl (1R)-1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate

There total 10 articles about tert-butyl (1R)-1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate 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: 95.0%

: 845829-92-7
tert-butyl (1R)-1-(4-bromo-2-fluorophenyl)ethylcarbamate

: 73183-34-3
bis(pinacol)diborane

: 845829-93-8
tert-butyl (1R)-1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate

Guidance literature:: With potassium acetate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In dichloromethane; dimethyl sulfoxide; at 90 ℃; for 50h;

Reference yield:

: 935431-10-0
N-[(1E)-(4-bromo-2-fluorophenyl)methylidene]-2-methylpropane-2-sulfinamide

: 845829-93-8
tert-butyl (1R)-1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1: 65 percent / CH₂Cl₂; diethyl ether / 1 h / -48 °C

2: 98 percent / HCl / dioxane; methanol

3: triethylamine / CH₂Cl₂ / 0 °C

4: 32.0 g / potassium acetate / [1,1'-bis(diphenylphosphino)ferrocene]PdCl₂ / dimethylsulfoxide / 3 h / 90 °C

With hydrogenchloride; potassium acetate; triethylamine; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; methanol; diethyl ether; dichloromethane; dimethyl sulfoxide;
DOI:10.1021/jm061094b

Reference yield:

: 925215-00-5
N-[(1R)-1-(4-bromo-2-fluorophenyl)ethyl]-2-methylpropane-2-sulfinamide

: 845829-93-8
tert-butyl (1R)-1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / HCl / dioxane; methanol

2: triethylamine / CH₂Cl₂ / 0 °C

3: 32.0 g / potassium acetate / [1,1'-bis(diphenylphosphino)ferrocene]PdCl₂ / dimethylsulfoxide / 3 h / 90 °C

With hydrogenchloride; potassium acetate; triethylamine; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; methanol; dichloromethane; dimethyl sulfoxide;
DOI:10.1021/jm061094b