(E)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide

Base Information

Chemical Name:(E)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide
CAS No.:1440434-21-8
Molecular Formula:C₂₁H₂₄N₂O₅
Molecular Weight:384.432
Hs Code.:

Synonyms:(E)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide

Suppliers and Price of (E)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide

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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)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide

Chemical Property:

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Technology Process of (E)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide

There total 5 articles about (E)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide 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:

: 1440434-16-1
N-(5-amino-2-hydroxyphenyl)-2-ethylbutanamide

: 77201-71-9
(E)-3-(3,4-dihydroxyphenyl)acryloyl chloride

: 1440434-21-8
(E)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide

Guidance literature:: With sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃; for 4h;
DOI:10.1016/j.bmcl.2013.04.033

Reference yield:

: 2736-40-5
chlorure d'acide ethyl-2 butyrique

: 1440434-21-8
(E)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydrogencarbonate / tetrahydrofuran; water / 20 °C / Cooling with ice

2: hydrogen; palladium 10% on activated carbon / methanol / 20 °C

3: sodium hydrogencarbonate / tetrahydrofuran; water / 4 h / 20 °C

With palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; In tetrahydrofuran; methanol; water;
DOI:10.1016/j.bmcl.2013.04.033

Reference yield:

: 331-39-5,501-16-6
caffeic acid

: 1440434-21-8
(E)-N-(5-(3-(3,4-dihydroxyphenyl)acrylamido)-2-hydroxyphenyl)-2-ethylbutanamide

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / tetrahydrofuran / Cooling with ice

2: sodium hydrogencarbonate / tetrahydrofuran; water / 4 h / 20 °C

With oxalyl dichloride; sodium hydrogencarbonate; N,N-dimethyl-formamide; In tetrahydrofuran; water;
DOI:10.1016/j.bmcl.2013.04.033