ethyl (E)-4-((benzoyloxy)(4-((tert-butoxycarbonyl)amino)butyl)amino)-4-oxobut-2-enoate

Base Information

Chemical Name:ethyl (E)-4-((benzoyloxy)(4-((tert-butoxycarbonyl)amino)butyl)amino)-4-oxobut-2-enoate
CAS No.:1447524-68-6
Molecular Formula:C₂₂H₃₀N₂O₇
Molecular Weight:434.489
Hs Code.:

Synonyms:ethyl (E)-4-((benzoyloxy)(4-((tert-butoxycarbonyl)amino)butyl)amino)-4-oxobut-2-enoate

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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 ethyl (E)-4-((benzoyloxy)(4-((tert-butoxycarbonyl)amino)butyl)amino)-4-oxobut-2-enoate

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Technology Process of ethyl (E)-4-((benzoyloxy)(4-((tert-butoxycarbonyl)amino)butyl)amino)-4-oxobut-2-enoate

There total 3 articles about ethyl (E)-4-((benzoyloxy)(4-((tert-butoxycarbonyl)amino)butyl)amino)-4-oxobut-2-enoate 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: 88.0%

: 66130-92-5
3-chlorocarbonylacrylic acid ethyl ester

: 1310809-19-8
tert-butyl (4-((benzoyloxy)amino)butyl)carbamate

: 1447524-68-6
ethyl (E)-4-((benzoyloxy)(4-((tert-butoxycarbonyl)amino)butyl)amino)-4-oxobut-2-enoate

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1039/c9cc06466d

Reference yield: 50.0%

: 1447524-68-6
ethyl (E)-4-((benzoyloxy)(4-((tert-butoxycarbonyl)amino)butyl)amino)-4-oxobut-2-enoate

Guidance literature:: With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 - 25 ℃; for 1.5h;

With dmap; triethylamine; In dichloromethane; at 0 - 25 ℃; for 2h;

Reference yield:

: 68076-36-8
1-amino-4-[(tert-butyloxycarbonyl)amino]butane

: 1447524-68-6
ethyl (E)-4-((benzoyloxy)(4-((tert-butoxycarbonyl)amino)butyl)amino)-4-oxobut-2-enoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate; sodium hydroxide / dichloromethane / 2.5 h / 20 °C / pH 10.5

2: triethylamine; dmap / dichloromethane / 2 h / 20 °C

With dmap; sodium hydrogencarbonate; triethylamine; sodium hydroxide; In dichloromethane;
DOI:10.1039/c9cc06466d