(E)-((E)-4-(2-methoxy-2-oxoethylidene)-2-(methoxycarbonyl)-3-(3-methoxyphenyl)cyclobut-2-enylidene)(3-methoxyphenyl)methyl 3-methoxybenzoate

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Chemical Name:(E)-((E)-4-(2-methoxy-2-oxoethylidene)-2-(methoxycarbonyl)-3-(3-methoxyphenyl)cyclobut-2-enylidene)(3-methoxyphenyl)methyl 3-methoxybenzoate
CAS No.:1160827-01-9
Molecular Formula:C₃₂H₂₈O₉
Molecular Weight:556.569
Hs Code.:

Synonyms:(E)-((E)-4-(2-methoxy-2-oxoethylidene)-2-(methoxycarbonyl)-3-(3-methoxyphenyl)cyclobut-2-enylidene)(3-methoxyphenyl)methyl 3-methoxybenzoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (E)-((E)-4-(2-methoxy-2-oxoethylidene)-2-(methoxycarbonyl)-3-(3-methoxyphenyl)cyclobut-2-enylidene)(3-methoxyphenyl)methyl 3-methoxybenzoate

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Technology Process of (E)-((E)-4-(2-methoxy-2-oxoethylidene)-2-(methoxycarbonyl)-3-(3-methoxyphenyl)cyclobut-2-enylidene)(3-methoxyphenyl)methyl 3-methoxybenzoate

There total 1 articles about (E)-((E)-4-(2-methoxy-2-oxoethylidene)-2-(methoxycarbonyl)-3-(3-methoxyphenyl)cyclobut-2-enylidene)(3-methoxyphenyl)methyl 3-methoxybenzoate 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: 42.0%

: 40101-17-5
3,3'-dimethoxybenzil

: 922-67-8
propynoic acid methyl ester

: 1160827-01-9
(E)-((E)-4-(2-methoxy-2-oxoethylidene)-2-(methoxycarbonyl)-3-(3-methoxyphenyl)cyclobut-2-enylidene)(3-methoxyphenyl)methyl 3-methoxybenzoate

: (3Z,4Z)-3,4-bis(2-methoxy-2-oxoethylidene)-1,2-bis(3-methoxyphenyl)cyclobutane-1,2-diyl bis(4-methoxybenzoate)

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; optical yield given as %de; diastereoselective reaction; Inert atmosphere; Cooling with ice;
DOI:10.1039/b819613c