tert-butyl (1-(4-(6-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate

Base Information

Chemical Name:tert-butyl (1-(4-(6-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate
CAS No.:1301610-94-5
Molecular Formula:C₃₀H₂₈N₂O₃
Molecular Weight:464.564
Hs Code.:

Synonyms:tert-butyl (1-(4-(6-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate

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Chemical Property of tert-butyl (1-(4-(6-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate

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Technology Process of tert-butyl (1-(4-(6-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate

There total 5 articles about tert-butyl (1-(4-(6-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate 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: 91.0%

: 1301610-93-4
tert-butyl (1-(4-(6-cyano-3-iodobenzofuran-2-yl)phenyl)cyclobutyl)carbamate

: 98-80-6
phenylboronic acid

: 1301610-94-5
tert-butyl (1-(4-(6-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: With cesium fluoride; palladium diacetate; triphenylphosphine; In 1,2-dimethoxyethane; at 75 ℃; for 5h;

Reference yield:

: 1032350-06-3
tert-butyl (1-(4-bromophenyl)cyclobutyl)carbamate

: 1301610-94-5
tert-butyl (1-(4-(6-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: diisopropylamine / copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 1,4-dioxane / 20 h / 20 - 80 °C / Inert atmosphere

2: potassium carbonate; methanol / 1 h

3: triethylamine / copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 18 h / 0 - 20 °C / Inert atmosphere

4: Iodine monochloride / dichloromethane / 0.5 h / 0 - 20 °C / Inert atmosphere

5: cesium fluoride / triphenylphosphine; palladium diacetate / 1,2-dimethoxyethane / 5 h / 75 °C

With methanol; Iodine monochloride; potassium carbonate; triethylamine; diisopropylamine; cesium fluoride; copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾; palladium diacetate; triphenylphosphine; In 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane;

Reference yield:

: 1301610-33-2
tert-butyl 1-(4-ethynylphenyl)cyclobutylcarbamate

: 1301610-94-5
tert-butyl (1-(4-(6-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 18 h / 0 - 20 °C / Inert atmosphere

2: Iodine monochloride / dichloromethane / 0.5 h / 0 - 20 °C / Inert atmosphere

3: cesium fluoride / triphenylphosphine; palladium diacetate / 1,2-dimethoxyethane / 5 h / 75 °C

With Iodine monochloride; triethylamine; cesium fluoride; copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾; palladium diacetate; triphenylphosphine; In 1,2-dimethoxyethane; dichloromethane;