(Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene

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Chemical Name:(Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene
CAS No.:247167-26-6
Molecular Formula:C₃₁H₃₈N₂O₁₀
Molecular Weight:598.65
Hs Code.:

(Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene

Synonyms:(Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene

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Chemical Property of (Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene

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Technology Process of (Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene

There total 3 articles about (Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene 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: 82.0%

: 2748-98-3
3-(4-formylphenoxy)-4-methoxybenzaldehyde

: 121056-95-9,89524-98-1
trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate

: 247167-26-6
(Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 20 ℃;
DOI:10.1016/S0040-4020(99)00576-1

Reference yield:

: 621-59-0
isovanillin

: 247167-26-6
(Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / potassium carbonate; copper(II) oxide / pyridine / 18 h / Heating

2: 82 percent / DBU / CH₂Cl₂ / 20 °C

With potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; copper(II) oxide; In pyridine; dichloromethane; 1: Ullmann coupling reaction / 2: Horner-Wadsworth-Emmons olefination;
DOI:10.1016/S0040-4020(99)00576-1

Reference yield:

: 1122-91-4
4-bromo-benzaldehyde

: 247167-26-6
(Z,Z)-4-{5-[2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl]-2-methoxyphenoxy}-1-{2-[(tert-butyloxycarbonyl)amino]-2-(methoxycarbonyl)ethenyl}benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / potassium carbonate; copper(II) oxide / pyridine / 18 h / Heating

2: 82 percent / DBU / CH₂Cl₂ / 20 °C

With potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; copper(II) oxide; In pyridine; dichloromethane; 1: Ullmann coupling reaction / 2: Horner-Wadsworth-Emmons olefination;
DOI:10.1016/S0040-4020(99)00576-1