tert-butyl 4-(2-(4-tert-butylphenyl)-3-oxocyclopent-1-enyl)phenylcarbamate

Base Information

Chemical Name:tert-butyl 4-(2-(4-tert-butylphenyl)-3-oxocyclopent-1-enyl)phenylcarbamate
CAS No.:1382250-34-1
Molecular Formula:C₂₆H₃₁NO₃
Molecular Weight:405.537
Hs Code.:

Synonyms:tert-butyl 4-(2-(4-tert-butylphenyl)-3-oxocyclopent-1-enyl)phenylcarbamate

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Chemical Property of tert-butyl 4-(2-(4-tert-butylphenyl)-3-oxocyclopent-1-enyl)phenylcarbamate

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Technology Process of tert-butyl 4-(2-(4-tert-butylphenyl)-3-oxocyclopent-1-enyl)phenylcarbamate

There total 5 articles about tert-butyl 4-(2-(4-tert-butylphenyl)-3-oxocyclopent-1-enyl)phenylcarbamate 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: 49.3%

: 1382250-32-9
3-bromo-2-(4-tert-butylphenyl)cyclopent-2-enone

: 330793-01-6
(4-tert-butoxycarbonylaminophenyl)boronic acid pinacol ester

: 1382250-34-1
tert-butyl 4-(2-(4-tert-butylphenyl)-3-oxocyclopent-1-enyl)phenylcarbamate

Guidance literature:: With potassium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; water; at 100 ℃; for 16h;

Reference yield:

: 3859-41-4
1,3-cyclopentadione

: 1382250-34-1
tert-butyl 4-(2-(4-tert-butylphenyl)-3-oxocyclopent-1-enyl)phenylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1: iodine / 16 h / 25 °C

2: N-Bromosuccinimide / dichloromethane / 16 h / 25 °C

3: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 16 h / 100 °C

4: phosphorus tribromide / 1,2-dichloro-ethane / 1 h / Reflux

5: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 16 h / 100 °C

With N-Bromosuccinimide; iodine; phosphorus tribromide; potassium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; dichloromethane; water; 1,2-dichloro-ethane;

Reference yield:

: 4683-50-5
3-methoxycyclopent-2-enone

: 1382250-34-1
tert-butyl 4-(2-(4-tert-butylphenyl)-3-oxocyclopent-1-enyl)phenylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide / dichloromethane / 16 h / 25 °C

2: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 16 h / 100 °C

3: phosphorus tribromide / 1,2-dichloro-ethane / 1 h / Reflux

4: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 16 h / 100 °C

With N-Bromosuccinimide; phosphorus tribromide; potassium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; dichloromethane; water; 1,2-dichloro-ethane;