{1-[4-(4-oxo-3-phenyl-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{1-[4-(4-oxo-3-phenyl-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester
CAS No.:1301611-03-9
Molecular Formula:C₃₀H₂₉NO₄
Molecular Weight:467.565
Hs Code.:

Synonyms:{1-[4-(4-oxo-3-phenyl-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

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Chemical Property of {1-[4-(4-oxo-3-phenyl-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

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Technology Process of {1-[4-(4-oxo-3-phenyl-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

There total 6 articles about {1-[4-(4-oxo-3-phenyl-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester 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: 100.0%

: 1301611-02-8
{1-[4-(3-iodo-4-oxo-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

: 98-80-6
phenylboronic acid

: 1301611-03-9
{1-[4-(4-oxo-3-phenyl-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Guidance literature:: With sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; water; at 130 ℃; for 0.5h; Inert atmosphere; Microwave irradiation;

Reference yield:

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

: 1301611-03-9
{1-[4-(4-oxo-3-phenyl-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

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

2.1: potassium carbonate; methanol / 1 h

3.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / -78 °C

3.2: 1.5 h / -78 - 20 °C

4.1: manganese(IV) oxide / dichloromethane / 18 h / 20 °C

5.1: Iodine monochloride / dichloromethane / 3.08 h / -78 - 20 °C / Inert atmosphere

6.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / 0.5 h / 130 °C / Inert atmosphere; Microwave irradiation

With methanol; manganese(IV) oxide; n-butyllithium; Iodine monochloride; sodium carbonate; potassium carbonate; diisopropylamine; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; bis(tri-t-butylphosphine)palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; hexane; dichloromethane; water;

Reference yield:

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

: 1301611-03-9
{1-[4-(4-oxo-3-phenyl-4H-chromen-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / -78 °C

1.2: 1.5 h / -78 - 20 °C

2.1: manganese(IV) oxide / dichloromethane / 18 h / 20 °C

3.1: Iodine monochloride / dichloromethane / 3.08 h / -78 - 20 °C / Inert atmosphere

4.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / 0.5 h / 130 °C / Inert atmosphere; Microwave irradiation

With manganese(IV) oxide; n-butyllithium; Iodine monochloride; sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,2-dimethoxyethane; hexane; dichloromethane; water;