C₃₀H₃₀N₂O₄

Base Information

Chemical Name:C₃₀H₃₀N₂O₄
CAS No.:1192129-04-6
Molecular Formula:C₃₀H₃₀N₂O₄
Molecular Weight:482.579
Hs Code.:

C<sub>30</sub>H<sub>30</sub>N<sub>2</sub>O<sub>4</sub>

Synonyms:C₃₀H₃₀N₂O₄

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Chemical Property of C₃₀H₃₀N₂O₄

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Technology Process of C₃₀H₃₀N₂O₄

There total 6 articles about C₃₀H₃₀N₂O₄ 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: 100.0%

: 1192127-66-4
C₂₃H₂₄N₂O₄*ClH

: 100-39-0
benzyl bromide

: 1192129-04-6
C₃₀H₃₀N₂O₄

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1016/j.ejmech.2013.03.061

Reference yield:

: 79099-07-3
N-tert-butyloxycarbonylpiperidin-4-one

: 1192129-04-6
C₃₀H₃₀N₂O₄

Guidance literature:: Multi-step reaction with 5 steps

1.1: pyrrolidine / 2 h / 72 °C / Microwave irradiation

2.1: triethylamine; palladium diacetate; tris-(o-tolyl)phosphine / N,N-dimethyl-formamide / 9 h / 100 °C / Inert atmosphere

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / Inert atmosphere

3.2: 3 h / 80 °C / Inert atmosphere

4.1: hydrogenchloride / 1,4-dioxane / 4 h / 20 °C

5.1: triethylamine / dichloromethane / 5 h / 20 °C

With pyrrolidine; hydrogenchloride; palladium diacetate; sodium hydride; triethylamine; tris-(o-tolyl)phosphine; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; mineral oil; 2.1: |Heck Reaction;
DOI:10.1016/j.ejmech.2013.03.061

Reference yield:

: 1192127-65-3
C₂₈H₃₂N₂O₆

: 1192129-04-6
C₃₀H₃₀N₂O₄

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / 1,4-dioxane / 4 h / 20 °C

2: triethylamine / dichloromethane / 5 h / 20 °C

With hydrogenchloride; triethylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1016/j.ejmech.2013.03.061