Acetic acid 4-((E)-2-{(1R,2R)-2-[(E)-3-(4-acetoxy-phenyl)-acryloylamino]-cyclohexylcarbamoyl}-vinyl)-phenyl ester

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Chemical Name:Acetic acid 4-((E)-2-{(1R,2R)-2-[(E)-3-(4-acetoxy-phenyl)-acryloylamino]-cyclohexylcarbamoyl}-vinyl)-phenyl ester
CAS No.:184866-91-9
Molecular Formula:C₂₈H₃₀N₂O₆
Molecular Weight:490.556
Hs Code.:

Synonyms:Acetic acid 4-((E)-2-{(1R,2R)-2-[(E)-3-(4-acetoxy-phenyl)-acryloylamino]-cyclohexylcarbamoyl}-vinyl)-phenyl ester

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Chemical Property of Acetic acid 4-((E)-2-{(1R,2R)-2-[(E)-3-(4-acetoxy-phenyl)-acryloylamino]-cyclohexylcarbamoyl}-vinyl)-phenyl ester

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Technology Process of Acetic acid 4-((E)-2-{(1R,2R)-2-[(E)-3-(4-acetoxy-phenyl)-acryloylamino]-cyclohexylcarbamoyl}-vinyl)-phenyl ester

There total 3 articles about Acetic acid 4-((E)-2-{(1R,2R)-2-[(E)-3-(4-acetoxy-phenyl)-acryloylamino]-cyclohexylcarbamoyl}-vinyl)-phenyl ester 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:

: 7400-08-0,50940-26-6
p-Coumaric Acid

: 184866-91-9
Acetic acid 4-((E)-2-{(1R,2R)-2-[(E)-3-(4-acetoxy-phenyl)-acryloylamino]-cyclohexylcarbamoyl}-vinyl)-phenyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / pyridine / 12 h / Ambient temperature

2: SOCl₂ / 3 h / Heating

3: (4-dimethylamino)pyridine, Et₃N / CH₂Cl₂ / 12 h / Ambient temperature

With pyridine; dmap; thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1016/0957-4166(96)00372-2

Reference yield:

: 27542-85-4
4-acetoxycinnamic acid

: 184866-91-9
Acetic acid 4-((E)-2-{(1R,2R)-2-[(E)-3-(4-acetoxy-phenyl)-acryloylamino]-cyclohexylcarbamoyl}-vinyl)-phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 3 h / Heating

2: (4-dimethylamino)pyridine, Et₃N / CH₂Cl₂ / 12 h / Ambient temperature

With dmap; thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1016/0957-4166(96)00372-2

Reference yield:

: 53901-95-4,108608-06-6,58523-18-5
p-acetoxycinnamoyl chloride

: 20439-47-8
(1R,2R)-1,2-diaminocyclohexane

: 184866-91-9
Acetic acid 4-((E)-2-{(1R,2R)-2-[(E)-3-(4-acetoxy-phenyl)-acryloylamino]-cyclohexylcarbamoyl}-vinyl)-phenyl ester

Guidance literature:: With dmap; triethylamine; In dichloromethane; for 12h; Yield given; Ambient temperature;
DOI:10.1016/0957-4166(96)00372-2