(E)-3-((4-phenyl-1,2,5-oxadiazol-3-yl)methoxy)benzyl 3-(4-(ethoxycarbonyloxy)-3-methoxyphenyl)acrylate

Base Information

Chemical Name:(E)-3-((4-phenyl-1,2,5-oxadiazol-3-yl)methoxy)benzyl 3-(4-(ethoxycarbonyloxy)-3-methoxyphenyl)acrylate
CAS No.:1257642-14-0
Molecular Formula:C₂₉H₂₆N₂O₉
Molecular Weight:546.533
Hs Code.:

Synonyms:(E)-3-((4-phenyl-1,2,5-oxadiazol-3-yl)methoxy)benzyl 3-(4-(ethoxycarbonyloxy)-3-methoxyphenyl)acrylate

Suppliers and Price of (E)-3-((4-phenyl-1,2,5-oxadiazol-3-yl)methoxy)benzyl 3-(4-(ethoxycarbonyloxy)-3-methoxyphenyl)acrylate

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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)-3-((4-phenyl-1,2,5-oxadiazol-3-yl)methoxy)benzyl 3-(4-(ethoxycarbonyloxy)-3-methoxyphenyl)acrylate

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Technology Process of (E)-3-((4-phenyl-1,2,5-oxadiazol-3-yl)methoxy)benzyl 3-(4-(ethoxycarbonyloxy)-3-methoxyphenyl)acrylate

There total 2 articles about (E)-3-((4-phenyl-1,2,5-oxadiazol-3-yl)methoxy)benzyl 3-(4-(ethoxycarbonyloxy)-3-methoxyphenyl)acrylate 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:

: 454170-81-1
C₁₆H₁₄N₂O₄

: 42381-67-9,62621-20-9
(2E)-3-{4-[(ethoxycarbonyl)oxy]-3-methoxyphenyl}acrylic acid

: 1257642-14-0
(E)-3-((4-phenyl-1,2,5-oxadiazol-3-yl)methoxy)benzyl 3-(4-(ethoxycarbonyloxy)-3-methoxyphenyl)acrylate

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃;
DOI:10.1002/ddr.20442

Reference yield:

: 1135-24-6,537-98-4
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid

: 1257642-14-0
(E)-3-((4-phenyl-1,2,5-oxadiazol-3-yl)methoxy)benzyl 3-(4-(ethoxycarbonyloxy)-3-methoxyphenyl)acrylate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / 4 h / 20 - 50 °C

2: dmap; dicyclohexyl-carbodiimide / dichloromethane / 20 °C

With dmap; dicyclohexyl-carbodiimide; sodium hydroxide; In dichloromethane;
DOI:10.1002/ddr.20442